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USRE37159E1 - Propanol derivatives and perfumes containing the same - Google Patents

Propanol derivatives and perfumes containing the same Download PDF

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USRE37159E1
USRE37159E1 US09/111,180 US11118098A USRE37159E US RE37159 E1 USRE37159 E1 US RE37159E1 US 11118098 A US11118098 A US 11118098A US RE37159 E USRE37159 E US RE37159E
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trimethylcyclohexan
optically active
perfume composition
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Tatsuya Ohmoto
Akemi Shimada
Takeshi Yamamoto
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Takasago International Corp
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Takasago International Corp
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Priority claimed from US07/879,738 external-priority patent/US5250512A/en
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C31/13—Monohydroxylic alcohols containing saturated rings
    • C07C31/133—Monohydroxylic alcohols containing saturated rings monocyclic
    • C07C31/135—Monohydroxylic alcohols containing saturated rings monocyclic with a five or six-membered rings; Naphthenic alcohols
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/29—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups
    • C07C45/298—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups with manganese derivatives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
    • C07C45/54—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition of compounds containing doubly bound oxygen atoms, e.g. esters
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/62—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by hydrogenation of carbon-to-carbon double or triple bonds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C47/00—Compounds having —CHO groups
    • C07C47/02—Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen
    • C07C47/105—Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen containing rings
    • C07C47/11—Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen containing rings monocyclic
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C47/00—Compounds having —CHO groups
    • C07C47/20—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
    • C07C47/225—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing rings other than six-membered aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C47/00—Compounds having —CHO groups
    • C07C47/28—Saturated compounds having —CHO groups bound to carbon atoms of rings other than six—membered aromatic rings
    • C07C47/32—Saturated compounds having —CHO groups bound to carbon atoms of rings other than six—membered aromatic rings with a six-membered ring
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B9/00—Essential oils; Perfumes
    • C11B9/0026—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring
    • C11B9/0034—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing six carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07—Optical isomers

Definitions

  • This invention relates to a novel propanol derivative useful for perfume cosmetics, etc., and a perfume containing the same as an active ingredient.
  • compounds known to have a wood-like fragrance or an amber-like fragrance include 1-(2,2,6-trimethylcyclohexan-1-yl)pentan-3-ol having an ethyl group as the alkyl moiety (see West German Patent Application (OLS) No.
  • JP-B-1-38438 discloses a composition of 1-(2,2,6-trimethylcyclohexan-1-yl)hexan-3-ol comprising 80% or more of a trans isomer and not more than 20% of a cis isomer.
  • an object of this invention is to provide an optically active compound which is capable of imparting an amber-like fragrance while meeting the above-described demand.
  • Another object of this invention is to provide a perfume comprising the above-described optically active compound as an active ingredient.
  • the inventors have conducted extensive investigations and, as a result, succeeded to synthesize an optically active isomer of a 3-(2,2,6-trimethylcyclohexan-1-yl)propanol derivative and found that the 6(S)-isomer of the compound has a sharp and highly diffusible amber fragrance free from a wood-like fragrance accompanied by the dim odor of mold and is useful as a perfume.
  • the present invention has been completed based on this finding.
  • the present invention relates to an optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanol derivative represented by formula (I):
  • R 1 represents a lower alkyl group.
  • the present invention further relates to a perfume containing the optically active compound of formula (I) as an active ingredient.
  • the lower alkyl group as represented by R 1 preferably contains from 1 to 4 carbon atoms, and specific examples thereof include a methyl group, and ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, and an isobutyl group.
  • R 1 is as defined above; and X represents a halogen atom.
  • the wavy line means a bond whose direction is not specified in the formula. It thus includes both the trans and cis forms of the compounds of formula ( I ) as reflected in Synthesis Examples 7 - 17 .
  • optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanol derivative of formula (I) can easily be synthesized by reacting an optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanal represented by formula (2) with an alkylmagnesium halide represented by the formula, R 1 MgX, wherein R 1 and X are the same as defined above.
  • R 2 represented a hydrogen atom or a methyl group
  • Ac represents an acetyl group
  • Et represents an ethyl group
  • the wavy line indicates a trans- and/or cis-position.
  • optically active 1-[6(S)-2,2,6-trimethylcyclohexan]carbaldehyde (5) as an intermediate compound of the above reaction route is known to by synthesized by starting with optically active citronellal as described in JP-A-63-44544, it can easily be synthesized in a high yield by starting with optically active 1-methoxycitronellal (3) which is used on an industrial scale as a perfume or juvenile pheromone of mosquito larvae. Namely, 1-methoxycitronellal (3) is reacted with acetic anhydride to obtain an enol acetate (4) which, as produced, is then subjected to cyclization in the presence of a phosphoric acid catalyst to obtain the compound (5).
  • the compound (5) is then reacted with triethyl phosphonoacetate (6) by utilizing the Wittig reaction described, e.g., In Herbert O. House, Modern Synthetic Reaction, p. 690, W. A. Benjamin, Inc., Menlo Park, Calif., U.S.A. (1972) by synthesize optically active ethyl 3-[6(S)-2,2,6-trimethylcyclohexan-1yl]acrylate (7).
  • the Wittig reaction described, e.g., In Herbert O. House, Modern Synthetic Reaction, p. 690, W. A. Benjamin, Inc., Menlo Park, Calif., U.S.A. (1972) by synthesize optically active ethyl 3-[6(S)-2,2,6-trimethylcyclohexan-1yl]acrylate (7).
  • the compound (7) is reduced by using sodium borohydride or sodium bis(2-methoxyethoxy)aluminum hydride to synthesize optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]-2-propen-1-ol (8) which is then oxidized with manganese dioxide to obtain optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]-2-propen-1-al (9).
  • the compound (9) is then hydrogenated in the presence of a palladium-on-carbon as a catalyst to synthesize optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanal (2).
  • the scent given off by the thus obtained 3-[2,2,6-trimethylcyclohexan-1-yl]propanol derivatives utterly differs between different optical antipodes.
  • the 6(S)-compounds have a sharp amber fragrance with very high diffusibility in common, though somewhat different in strength and quality depending on the kind of R 1 .
  • the 6(R)-compounds basically produce no amber fragrance and give off a powerless wood-like fragrance with a little moldiness. The racemates give off a dull woody amber fragrance which is remarkably different from and far less powerful than that of the 6(S)-compounds.
  • each of the 6(S)-compounds differing in R 1 was proved effective to impart to a perfume composition a distinct top note to yield a fresher and tastier composition as though it is of different kind from the corresponding 6(R)-compound or racemate. It was also proved that the 6(S)-compounds have high fragrance retention and high masking effects over odors of bases of soaps, etc., odors of bleaching agents, and ozone odor and are, therefore, very useful as perfume materials.
  • a fresh and tasty fragrance or a fragrance modifying or strengthening agent with high diffusibility and retention which contains the 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanol derivative according to the present invention.
  • cosmetics, sanitary goods, pharmaceuticals, etc. which contains the compound of the invention as a perfume component.
  • the compound according to the present invention can be incorporated in an amount effective to impart its unique fragrance into bases of hair care cosmetics, e.g., shampoos, rinses, perfumes, colognes, hair tonics, hair creams, pomades, etc.; bases of facial cosmetics, e.g., face powders, lip sticks, etc.; toilet foods, e.g., face cleansers, soaps, disinfectants, tooth pastes, mouth-washes, toilet paper, etc.; various detergents, e.g., dish washing detergents, laundry detergents, textile softeners, disinfectant detergents, deodorant detergents, bleaching agent, etc.; environmental aromatizers, furniture care goods, insecticides; flavors for facilitating administration of medicines; and the like thereby to enhance the commercial value of these goods.
  • hair care cosmetics e.g., shampoos, rinses, perfumes, colognes, hair tonics, hair creams, pomades, etc.
  • bases of facial cosmetics e.g.,
  • a suitable amount of the propanol derivative according to the present invention which is used in a perfume composition to be applied to various products is from 0.0001 to 50% by weight and preferably from 0.001 to 20% by weight.
  • reaction mixture was refluxed at 101° to 117° C. for 6-hours, followed by cooling to 5° C.
  • 500 g of water and 500 g of toluene were added to the reaction mixture to conduct water washing and liquid-liquid separation. Again, 500 g of water was added thereto to conduct water washing and liquid-liquid separation to obtain 1,690 g of a toluene solution of an enol acetate (4).
  • the reaction mixture was cooled to 5° C. and washed with 2,000 ml of cold water, followed by water washing and liquid-liquid separation. The mixture was further washed and separated successively with 2,000 ml of water, 2,000 ml of a 5% soda ash aqueous solution, and 2,000 ml of a saturated sodium chloride aqueous solution.
  • the toluene was removed by distillation under reduced pressure to obtain 872 g of a concentrated oil.
  • the resulting concentrated oil was subjected to rectification using a 1 mm distillation column packed with Helipack to obtain 425 g of optically active 1-[6(S)-2,2,6-trimethylcyclohexan]carbaldehyde (5).
  • Boiling point 80°-81° C./8 mmHg
  • reaction mixture was worked up in a usual manner to obtain 390 g of a concentrated oil which was then purified by rectification using a 30 cm Helipack-packed distillation column to obtain 322 g of optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]-2-propen-1-ol (8).
  • Boiling point 95°-96° C./0.95 mmHg
  • reaction mixture was worked up in a usual manner, and 17 g of the resulting concentrated oil was subjected to rectification using a 20 cm Helipack-packed distillation column to obtain 13 g of optically active 1-[6(S)-2,2,6-trimethylcyclohexan-1-yl]butan-3-ol (12).
  • reaction mixture was worked up in a usual manner, and the resulting concentrated oil (18 g) was subjected to rectification by using a 20 cm Helipack-packed distillation column to obtain 13 g of optically active 1-[6(S)-2,2,6-trimethylcyclohexan-1-yl]hexan-3-ol (16).
  • Boiling point 98°-101° C./1 mmHg
  • Boiling point 98°-101° C./1 mmHg
  • Boiling point 109°-110° C./1 mmHg
  • Boiling point 109°-110° C./1 mmHg
  • Odor evaluation was carried out by a panel of 5 specialists on the 6(S)-compound, 6(R)-compound, and racemate of each of the 3-(2,2,6-trimethylcyclohexan-1-yl)propanal derivatives having various alkyl groups as R: as synthesized in the foregoing Synthesis Examples. The results are shown in Tables 1 and 2 below. Standards of rating were as follows.
  • a shampoo composition containing 1-[6(S)-2,2,6-trimethylcyclohexan-1-yl]heptane-3-ol or a racemate thereof as shown in Table 3 below was prepared, and the degree of masking was evaluated by a panel of 5 specialists. As a result, the panel judged that Composition A containing the optically active compound smelled pleasantly of amber with the base odor being perfectly masked; Composition B containing the racemate smelled considerably of the base; and the smell of the base was substantially overpowered in Composition C containing the racemate in an amount 8 times that of the optically active compound in Composition A.
  • the panel judged that: B-1 containing the optically active compound and B-4 containing the racemate in an amount 9 times that of the optically active compound in B-1 had an almost equal strength of fragrance, the top note of B-4 being, however, broadwise spreading and lacking sharpness, while B-1 had a well-balanced fragrance with freshness and was preferred to B-4.
  • B-2, B-3, and B-4 the panel judged that the strength of fragrance was decreasing in the order of B-4>B-3>B-2 and that the preference was also decreasing in the same order.
  • a white floral perfume Composition (A) or (B) for detergents having the following formulation was prepared.
  • a green floral and highly preferably perfume composition for shampoo having the following formulation was prepared.
  • a highly preferable Fougere type perfume composition for textile softeners having the following formulation was prepared.
  • a liquid hypochlorite bleaching agent having the following formulation was prepared.
  • Composition (A) or (B) having an amber fragrance was added to the liquid hypochlorite bleaching solution in an amount of 0.1% or 0.2%, respectively to prepare Composition (A) or (B) having an amber fragrance.
  • composition (A) and (B) The degree of masking of the odor of the hypochlorite in each of Compositions (A) and (B) was tested by a panel of 5 specialists. As a result, the panel judged that Composition (A) had a fresh amber-like fragrance with no perceptible odor of the hypochlorite, whereas Composition (B) smelled slightly of the hypochlorite.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Fats And Perfumes (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

An optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanol derivative represented by formula (I):
Figure USRE037159-20010501-C00001
wherein R1 represents a lower alkyl group, and a perfume containing the same as an active ingredient are disclosed.

Description

This is a Continuation of Application No. 07/592,099 filed Oct. 3, 1990 abandoned.
FIELD OF THE INVENTION
This invention relates to a novel propanol derivative useful for perfume cosmetics, etc., and a perfume containing the same as an active ingredient.
BACKGROUND OF THE INVENTION
Some naturally-occurring compounds exhibit various characteristics attributed to their asymmetric structure. Of physiologically active substances having an asymmetric structure, many of those useful for humans are confined to the respective specific antipode. This tendency is particularly conspicuous in the field of pharmaceuticals, agricultural chemicals, pheromones, and food additives. It is known in these fields that a racemic mixture may have a markedly reduced effect or rather exhibit a counter effect. The field of perfumes is no exception to this tendency. For example, 1-menthol has the odor of mint; d-carvone has the odor of Caraway L.; and d-nootkatone has the odor of grapefruit. Each of these optical antipodes is different from or stronger than the respective other optical antipodes in odor. The latest examples of such a phenomenon are observed in α-ionine, hydroxycitronellal, and rose oxide. For the detail, reference can be made to Kaqaku Sosetsu, No. 14, Ch. 6 “Aji to Nioi no Kagaku” (1976).
Therefore, development of optically active perfume components as well as development of novel perfumes would lead to development of optical antipodes having a new odor or usefulness and are of industrial significance.
With respect to 3-(2,2,6-trimethylcyclohexan-1-yl)propanol derivatives, compounds known to have a wood-like fragrance or an amber-like fragrance include 1-(2,2,6-trimethylcyclohexan-1-yl)pentan-3-ol having an ethyl group as the alkyl moiety (see West German Patent Application (OLS) No. 2,455,761), 1-(2,2,6-trimethylcyclohexan-1-yl)hexan-3-ol having a propyl group as the alkyl moiety (see JP-A-62-70314, JP-B-1-38438, JP-B-59-18373, JP-A-61-191636, and JP-B-62-16935; the terms “JP-A” and “JP-B” as used herein mean an “unexamined published Japanese patent application” and an “examined Japanese patent publication”, respectively), and 5-methyl-1-(2,2,6-trimethylcyclohexan-1-yl(hexan-3-ol having an isobutyl group as the alkyl moiety (See USSR Patent 1,082,780).
JP-B-1-38438 discloses a composition of 1-(2,2,6-trimethylcyclohexan-1-yl)hexan-3-ol comprising 80% or more of a trans isomer and not more than 20% of a cis isomer.
Since these cis and trans isomers each has an asymmetric carbon atom in the molecule thereof, it is expected that there are a pair of enantiomers, i.e., (+)-isomer and (−)-isomer. However, the compounds disclosed in the above-cited references exist as a racemic mixture. No other study has been reported on synthesis or properties of the individual optical isomers.
The recent diversity of cosmetics and sanitary goods has created a new increasing demand for a perfume material which has a high diffusibility, unique scent, high tastiness, high retention, satisfactory stability, and high safety. In particular, perfume materials having an amber-like fragrance and satisfying these requirements have been wanted.
SUMMARY OF THE INVENTION
Accordingly, an object of this invention is to provide an optically active compound which is capable of imparting an amber-like fragrance while meeting the above-described demand.
Another object of this invention is to provide a perfume comprising the above-described optically active compound as an active ingredient.
In the light of the above-mentioned circumstances, the inventors have conducted extensive investigations and, as a result, succeeded to synthesize an optically active isomer of a 3-(2,2,6-trimethylcyclohexan-1-yl)propanol derivative and found that the 6(S)-isomer of the compound has a sharp and highly diffusible amber fragrance free from a wood-like fragrance accompanied by the dim odor of mold and is useful as a perfume. The present invention has been completed based on this finding.
The present invention relates to an optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanol derivative represented by formula (I):
Figure USRE037159-20010501-C00002
wherein R1 represents a lower alkyl group.
The present invention further relates to a perfume containing the optically active compound of formula (I) as an active ingredient.
DETAILED DESCRIPTION OF THE INVENTION
In formula (I), the lower alkyl group as represented by R1 preferably contains from 1 to 4 carbon atoms, and specific examples thereof include a methyl group, and ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, and an isobutyl group.
The optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanol derivative of formula (I) can be synthesized, for example, in the following reaction scheme.
Figure USRE037159-20010501-C00003
wherein R1 is as defined above; and X represents a halogen atom.
The above active optically active propanol derivatives of formula (I) can also be represented by the following formula (A):
Figure USRE037159-20010501-C00004
In the above formula (A), the wavy line means a bond whose direction is not specified in the formula. It thus includes both the trans and cis forms of the compounds of formula (I) as reflected in Synthesis Examples 7-17.
That is, the optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanol derivative of formula (I) can easily be synthesized by reacting an optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanal represented by formula (2) with an alkylmagnesium halide represented by the formula, R1MgX, wherein R1 and X are the same as defined above.
The starting compound, 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanal (2), is a novel compound and can be synthesized in the following reaction scheme:
Figure USRE037159-20010501-C00005
wherein R2 represented a hydrogen atom or a methyl group; Ac represents an acetyl group; Et represents an ethyl group; and the wavy line indicates a trans- and/or cis-position.
While an optically active 1-[6(S)-2,2,6-trimethylcyclohexan]carbaldehyde (5) as an intermediate compound of the above reaction route is known to by synthesized by starting with optically active citronellal as described in JP-A-63-44544, it can easily be synthesized in a high yield by starting with optically active 1-methoxycitronellal (3) which is used on an industrial scale as a perfume or juvenile pheromone of mosquito larvae. Namely, 1-methoxycitronellal (3) is reacted with acetic anhydride to obtain an enol acetate (4) which, as produced, is then subjected to cyclization in the presence of a phosphoric acid catalyst to obtain the compound (5).
The compound (5) is then reacted with triethyl phosphonoacetate (6) by utilizing the Wittig reaction described, e.g., In Herbert O. House, Modern Synthetic Reaction, p. 690, W. A. Benjamin, Inc., Menlo Park, Calif., U.S.A. (1972) by synthesize optically active ethyl 3-[6(S)-2,2,6-trimethylcyclohexan-1yl]acrylate (7).
The compound (7) is reduced by using sodium borohydride or sodium bis(2-methoxyethoxy)aluminum hydride to synthesize optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]-2-propen-1-ol (8) which is then oxidized with manganese dioxide to obtain optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]-2-propen-1-al (9). The compound (9) is then hydrogenated in the presence of a palladium-on-carbon as a catalyst to synthesize optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanal (2).
While the above description relates to synthesis of the 6(S)-compound, a 6(R)-compound can be obtained in the similar manner by starting with d-methoxycitronellal in place of 1-methoxycitronellal.
It surprisingly turned out that the scent given off by the thus obtained 3-[2,2,6-trimethylcyclohexan-1-yl]propanol derivatives utterly differs between different optical antipodes. More specifically, the 6(S)-compounds have a sharp amber fragrance with very high diffusibility in common, though somewhat different in strength and quality depending on the kind of R1. On the other hand, the 6(R)-compounds basically produce no amber fragrance and give off a powerless wood-like fragrance with a little moldiness. The racemates give off a dull woody amber fragrance which is remarkably different from and far less powerful than that of the 6(S)-compounds.
Further, each of the 6(S)-compounds differing in R1 was proved effective to impart to a perfume composition a distinct top note to yield a fresher and tastier composition as though it is of different kind from the corresponding 6(R)-compound or racemate. It was also proved that the 6(S)-compounds have high fragrance retention and high masking effects over odors of bases of soaps, etc., odors of bleaching agents, and ozone odor and are, therefore, very useful as perfume materials.
Thus, there is provided a fresh and tasty fragrance or a fragrance modifying or strengthening agent with high diffusibility and retention, which contains the 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanol derivative according to the present invention. There are also provided cosmetics, sanitary goods, pharmaceuticals, etc., which contains the compound of the invention as a perfume component. That is, the compound according to the present invention can be incorporated in an amount effective to impart its unique fragrance into bases of hair care cosmetics, e.g., shampoos, rinses, perfumes, colognes, hair tonics, hair creams, pomades, etc.; bases of facial cosmetics, e.g., face powders, lip sticks, etc.; toilet foods, e.g., face cleansers, soaps, disinfectants, tooth pastes, mouth-washes, toilet paper, etc.; various detergents, e.g., dish washing detergents, laundry detergents, textile softeners, disinfectant detergents, deodorant detergents, bleaching agent, etc.; environmental aromatizers, furniture care goods, insecticides; flavors for facilitating administration of medicines; and the like thereby to enhance the commercial value of these goods.
A suitable amount of the propanol derivative according to the present invention which is used in a perfume composition to be applied to various products is from 0.0001 to 50% by weight and preferably from 0.001 to 20% by weight.
The present invention is now illustrated in greater detail with reference to Synthesis Examples and Examples. All the parts, percents, and ratios are by weight unless otherwise indicated.
SYNTHESIS EXAMPLE 1 Synthesis of 1-[6(S)-2,2,6-Trimethylcyclohexan]carbaldehyde (5)
In a 5 l-volume four-necked flask equipped with a condenser, a thermometer, a dropping funnel, and a stirrer were charged 871 g of acetic anhydride, 27 g of sodium acetate, and 706 g of triethylamine under a nitrogen atmosphere, and the mixture was heated to 75° C. while stirring. To the resulting solution was added dropwise 1 kg of 1-methoxycitronellal (a commercially available product of Takasago International Corporation; [α]D 25: −10.42°; optical purity: 98% ee) over 1 hour.
After the dropwise addition, the reaction mixture was refluxed at 101° to 117° C. for 6-hours, followed by cooling to 5° C. To the reaction mixture were added 500 g of water and 500 g of toluene to conduct water washing and liquid-liquid separation. Again, 500 g of water was added thereto to conduct water washing and liquid-liquid separation to obtain 1,690 g of a toluene solution of an enol acetate (4). Gas chromatography (“HEWLETT PACKARD 5890”; column; Carbowax 20M (HP); 0.2 mm ID×25 m) (hereinafter abbreviated as GC) revealed that the solute was composed of 29.5% of cis-compound (4), 62.75% of trans-compound (4), and 5.3% of diacetate (10).
Figure USRE037159-20010501-C00006
wherein Me represents a methyl group; and Ac represents an acetyl group. Spectral Data: Mass (CI)
(4)-Trans: 229 (M + 1,1), 197 (70), 155 (42), 137 (100),
95 (12), 73 (41)
(4)-Cis: 229 (M + 1,3), 197 (100), 155 (88), 137 (98),
95 (24), 73 (82)
(10): 289 (M + 1,0.2), 197 (85), 155 (75), 137 (100),
103 (19), 73 (33)
In a 5 l-volume four-necked flask equipped with a condenser, a thermometer, an outlet for water, and a stirrer were charged 1,690 g of the resulting toluene solution of compound (4), 620 g of 85% phosphoric acid, and 500 g of toluene, and the mixture was heat-refluxed at 71° to 107° C. for 3 hours with stirring under a nitrogen atmosphere while controlling the refluxing temperature by removing the produced methanol together with toluene in small portions.
The reaction mixture was cooled to 5° C. and washed with 2,000 ml of cold water, followed by water washing and liquid-liquid separation. The mixture was further washed and separated successively with 2,000 ml of water, 2,000 ml of a 5% soda ash aqueous solution, and 2,000 ml of a saturated sodium chloride aqueous solution. The toluene was removed by distillation under reduced pressure to obtain 872 g of a concentrated oil. The resulting concentrated oil was subjected to rectification using a 1 mm distillation column packed with Helipack to obtain 425 g of optically active 1-[6(S)-2,2,6-trimethylcyclohexan]carbaldehyde (5).
Boiling point: 80°-81° C./8 mmHg
[α]D 25: −0.47°
Purity by GC: (5)-Trans: 90%; (5)-Cis: 10%
Figure USRE037159-20010501-C00007
SYNTHESIS EXAMPLE 2 Synthesis of Ethyl 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]acrylate (7)
In a 10 l-volume four-necked flash equipped with a condenser, a thermometer, a dropping funnel, and a stirrer were charged 1,000 g of a sodium hydride dispersion (purity: 60% and 3,400 ml of tetrahydrofuran, and 565 g of triethyl phosphonoacetate (6) was added dropwise thereto over 1 hours. The mixture was stirred for 1 hour until hydrogen gas was not evolved.
Then, 424 g of the compound (5) prepared in Synthesis Example 1 was added dropwise thereto at room temperature over 1 hour, followed by stirring at room temperature for 3 hours to complete the reaction. To the reaction mixture was added 1 kg of water to conduct water washing and liquid-liquid separation, followed by working up in a usual manner to obtain 526 g of a concentrated oil.
The resulting concentrated oil was subjected to rectification using a 30 cm Helipack-packed distillation column to obtain 465 g of optically active ethyl 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]acrylate (7).
Boiling point: 108-109° C./0.95.mmHg
[α]D 25: +21.41°
Purity by GC: 99.5% (the product was not separated into the cis and trans compounds.)
Spectral Data of Compound (7):
1HNMR (400 MHz, CDCl3, δ): 0.75 (3H, d, J=4.3 Hz), 0.82 (3H, s), 0.88 (3H, s), 1.29 (3H, t, J=7.1 Hz), 0.89-1.8 (8H), 4.18 (2H, q, J=7.1 Hz), 5.76 (1H, d, J=15.5 Hz), 6.73 (1H, q, J=15.5 Hz, J=10.1 Hz)
MS m/e: 224 (M+, 18), 209 (7), 179 (25 ), 168 (9), 150 (37), 136 (100), 125 (23), 109 (50), 95 (75), 81 (64), 69 (70), 55 (35), 41 (16), 29 (11)
IR νmax (cm−1): 2925, 1720, 1650, 1365, 1150-1180
SYNTHESIS EXAMPLE 3 Synthesis of 3-[6(S)-2,2,6-Trimethylcyclohexan-1-yl]-2-propen-1-ol (8)
Into a 5 l-volume four-necked flask equipped with a condenser, a thermometer, a dropping funnel, and a stirrer were charged 633 g of a 70% toluene solution of sodium bis(2-methoxyethoxy)aluminum hydride and 2,100 ml of toluene under a nitrogen atmosphere, and 460 g of the compound (7) prepared in Synthesis Example 2 was added dropwise to the mixture at room temperature over 2 hours, followed by stirring at that temperature for 1 hour to complete the reaction.
The reaction mixture was worked up in a usual manner to obtain 390 g of a concentrated oil which was then purified by rectification using a 30 cm Helipack-packed distillation column to obtain 322 g of optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]-2-propen-1-ol (8).
Boiling point: 95°-96° C./0.95 mmHg
[α]D 25: +23.33°
Purity by GC: (8)-Trans: 95%; (8)-Cis: 5%
Figure USRE037159-20010501-C00008
Spectral Data of (8)-Trans:
1H-NMR (400 MHz, CDC3, δ): .76 (3H, d, J=6.3 Hz), 0.82 (6H, s), 0.87-1.49 (8H), 1.69 (1H, m), 4.11 (2H, q, Jgem=1.3 Hz, Jvic=5.9 Hz), 5.39 (1H, m), 5.57 (1H, m)
MS m/e: 182 (M+, 2), 164 (4), 149 (18), 138 (12), 124 (39), 109 (52), 95 (70), 81 (63), 69 (100), 55 (57), 41 (22), 28 (6)
IR νmax(cm−1): 3325, 2920, 1365, 970
Spectral Data of (8)-Cis:
MS m/e: 182 (M30, 3), 164 (7), 149 (18), 138 (11), 124 (48), 109 (74), 95 (78), 81 (50), 69 (100), 55 (46), 41 (24), 32 (9.6)
SYNTHESIS EXAMPLE 4 Synthesis of 3-[6(S)-2,2,6-Trimethylcyclohexan-1-yl]-2-propen-1-al (9)
In a 2 l-volume four-necked flask equipped with a thermometer and a stirrer were charged 4,300 g of activated manganese dioxide, 10 l of n-octane, and 320 g of the compound (8) synthesized in Synthesis Example 3, and the mixture was stirred at 40° to 45° C. for 12 hours to complete the reaction. The reaction mixture was filtered and concentrated to obtain 326 g of a concentrated oil which was then purified by rectification by using a 30 cm Helipack-packed distillation column to obtain 277 g of optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]-2-propen-1-al (9).
Boiling point: 90°-91° C./0.9 mmHg
[α]D 25: +33.44°
Purity by GC: (9)-Trans: 95.5%; (9)-Cis: 4.5%
Figure USRE037159-20010501-C00009
Spectral Data of (9)-Trans:
1H-NMR (400 MHz, CDCl3, δ): 0.76 (3H, d, J=2.4 Hz), 0.91 (3H, s), 0.84 (3H, s), 1.22-1.71 (8H), 6.08 (1H, q, J=15.5 Hz, J=8 Hz), 6.61 (1H, q, J=15.5Hz, J=10.1Hz), 9.52 (1H, d, J=8Hz)
MS m/e: 180 (M+, 13), 165(11), 147 (6), 137 (43), 123 (31), 109 (41) 95 (100) 81 (72) 69 (35) 55 (30), 41 (24 )
IR νmax (cm−1): 2920, 2860, 2840, 1680, 1460, 1370, 1120, 1110
Spectral Data of (9)-Cis:
MS m/e: 180 (M+, 11), 165 (11), 147 (4), 137 (43), 123 (33), 109 (31), 95 (100), 81 (51), 69 (26), 55 (26), 41 (20)
SYNTHESIS EXAMPLE 5 Synthesis of 3-[6(S)-2,2,6-Trimethylcyclohexan-1-yl]propanal (2)
In 7 l of ethanol was added 276 g of the compound (9) synthesized in Synthesis Example 4, and the mixture was subjected to hydrogenation at room temperature at atmospheric pressure using 14 g of 5% paladium-on-carbon as a catalyst. After the reaction, the catalyst was removed by filtration, and the resulting 290 g of a concentrated oil was purified by rectification using a 30 cm Helipack-packed distillation column to obtain 242 g of optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanal (2).
Boiling point: 93°-94° C./1.1 mmHg
[α]D 25: +11.88°
Purity by GC: (2)-Trans: 95.7%; (2)-Cis: 4.3%
Figure USRE037159-20010501-C00010
Spectral Data of (2)-Trans:
1HNMR (400 MHz, CDCl3, δ): 0.80 (3H, d, J=4.3 Hz), 0.90 (6H), 0.92-1.78 (8H), 2.27-2.53 (4H), 9.74 (1H, t, J=1.9 Hz)
MS m/e 182 (M+, 8), 167 (12), 149 (16), 138 (17), 123 (13), 109 (35), 95 (17), 82 (70), 69 (100), 55 (48), 41 (20)
IR νmax (cm−1): 2920, 2890, 2840, 1720, 1460, 1390, 1380
Spectral Data of (2)-Cis:
MS m/e: 182 (M+, 4), 167 (7), 149 (16), 138 (52), 123 (68), 109 (41), 95 (76), 82 (98), 69 (100), 55 (52), 41 (18), 29 (41), 18 (9)
SYNTHESIS EXAMPLE 6 Synthesis of 3-[6(R)-2,2,6-Trimethylcyclohexan-1-yl]propanal (11)
The same procedures as in Synthesis Examples 1 through 5 were repeated, except for replacing the starting 1-methoxycirtonellal with d-methoxycitronellal (a commercially available product sold by Takasago International Corporation; [α]D 25: +10.42°; optical purity: 98% ee), to obtain 240 g of optically active 3-[6(R)-2,2,6-trimethylcyclohexan-1-yl]propanal (11).
Boiling point: 93-94° C./1.1 mmHg
[α]D 25-11.87°
Purity by GC: (11)-Trans: 95.6%; (11)-Cis: 4.4%
Figure USRE037159-20010501-C00011
SYNTHESIS EXAMPLE 7 Synthesis of 1-[6(S)-2,2,6-Trimethylcyclohexan-1-yl]butan-3-ol (12)
In a 300 ml-volume four-necked flask equipped with a condenser, a thermometer, a dropping funnel, a gas blowing tube, and a stirrer were charged 5.0 g of a magnesium powder, 0.001 g of iodine, 0.5 g of methyl iodide, and 10 ml of tetrahydrofuran under a nitrogen atmosphere. After confirming the start of a Grignard reaction (generation of bubbling), of tetrahydrofuran was added thereto, and methyl chloride gas was blown into the reaction mixture at 40° to 45° C. for 4 hours with stirring until the magnesium powder disappeared to thereby prepare a tetrahydrofuran solution of methylmagnesium chloride. To the resulting solution was added dropwise a solution of 15 g of the 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanal (2) obtained in Synthesis Example 5 in 15 ml of tetrahydrofuran at 5° C. over 2 hours, followed by stirring at that temperature for 4 hours to complete the reaction. The reaction mixture was worked up in a usual manner, and 17 g of the resulting concentrated oil was subjected to rectification using a 20 cm Helipack-packed distillation column to obtain 13 g of optically active 1-[6(S)-2,2,6-trimethylcyclohexan-1-yl]butan-3-ol (12).
Boiling point: 93°-95° C./1 mmHg
[α]D 25: +12.98°Purity by GC: (12)-Trans: 95.3%; (12)-Cis: 4.7%
Elemental analysis:
Calcd. (%) C: 78.72; H: 13.21; O: 8.07
Found (%) C: 78.71; H: 13.22; O: 8.07
Figure USRE037159-20010501-C00012
Spectral Data of (12)-Trans:
1HNMR (400 MHz, CDCl3, δ): 3.75 (1H, m), 1.19 (3H, d, J=6.17 Hz), 0.88 (3H, d, J=6 Hz), 0.89 (3H, s), 0.79 (3H, s), 0.55 (1H, m), 1.6-0.9 (12H, m)
MS m/e: 198 (M+, 1), 180 (8), 165 (13), 151 (1), 138 (13), 124 (40), 109 (65), 95 (59), 82 (53), 69 (100), 55 (49), 45 (27), 29 (1)
IR νmax (cm−1): 3348, 1460, 1375, 1100
Spectral Data of (12)-Cis:
MS m/e: 198 (0), 180 (4), 165 (24), 138 (20), 123 (39), 109 (59), 95 (61), 82 (67), 69 (100), 55 (59), 43 (30), 32 (5)
SYNTHESIS EXAMPLE 8 Synthesis of 1-[6(R)-2,2,6-Trimethylcyclohexan-1-yl]butan-3-ol (13)
The same procedure as in Synthesis Example 7 was repeated, except for replacing the starting 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanal with 10 g of 3-[6(R)-2,2,6-trimethylcyclohexan-1-yl]propanal, to obtain 9 g of optically active 1-[6(R)-2,2,6-trimethylcyclohexan-1-yl]butan-3-ol (13).
Boiling point 93°-95° C./1 mmHg
[α]D 25: −12.96°
Purity by GC: (13)-Trans: 95.2%; (13)-Cis: 4.8%
Elemental Analysis: Calcd. (%) C: 79.57; H: 13.36; O: 7.07 Found (%) C: 79.54; H: 13.37; O: 7.09
Figure USRE037159-20010501-C00013
SYNTHESIS EXAMPLE 9 Synthesis of 1-[6(S)-2,2,6-Trimethylcyclohexan-1-yl]pentan-3-ol (14)
The same procedure as in Synthesis Example 7 was repeated, except for replacing the methyl iodide and methyl chloride gas with ethyl iodide and ethyl chloride gas, respectively to prepare a tetrahydrofuran solution of ethylmagnesium chloride. The resulting concentrated oil (17 g) was subjected to rectification by using a 20 cm Helipack-packed distillation column to obtain 13 g of optically active 1-[6(S)-2,2,6-trimethylcyclohexan-1-yl]pentan-3-ol (14).
Boiling point: 95°-97° C./1 mmHg
[α]D 25: +13.08°
Purity by GC: (14)-Trans: 95.0%; (14)-Cis: 5.0%
Elemental Analysis: Calcd. (%) C: 79.18; H: 13.29; O: 7.53 Found (%) C: 79.12; H: 13.32; O: 7.56
Figure USRE037159-20010501-C00014
Spectral Data of (14)-Trans:
1HNMR (400 MHz, CDCl3, δ): 0.54 (1H, m), 0.79 (3H, s), 0.88-0.96 (10H), 1.00-1.66 (13H), 3.48 (1H, m)
MS m/e: 194 (M-18, 16), 179 (17), 165 (4), 151 (4), 138 (46), 124 (56), 109 (87), 95 (59), 82 (56), 69 (100), 55 (41), 41 (13), 31 (3), 82 (56), 69 (100), 55 (41), 41 (13), 31 (3)
IR νmax (cm−1): 3340, 2920, 2865, 2840, 1460, 1387, 1367
Spectral Data of (14)-Cis:
MS m/e: 194 (M-18), 179 (55), 165 (4), 151 (6), 138 (45), 123 (80), 109 (91), 95 (76), 82 (7), 69 (100), 55 (41), 41 (12), 31 (4)
SYNTHESIS EXAMPLE 10 Synthesis of 1-[6(R)-2,2,6-Trimethylcyclohexan-1-yl]pentan-3-ol (15)
The same procedure as in Synthesis Example 7 was repeated, except for replacing the methyl iodide and methyl chloride gas with ethyl iodide and ethyl chloride gas, respectively to prepare a tetrahydrofuran solution of ethylmagnesium chloride and replacing 15 g of the starting 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanal with 10 g of 3-[6(R)-2,2,6-trimethylcyclohexan-1-yl]propanal, to obtain 9 g of optically active 1-[6(R)-2,2,6-trimethylcyclohexan-1-yl]pentan-3-ol (15).
Boiling point: 95°-97° C./1 mmHg
[α]D 25: −13.08°
Purity by GC: (15)-Trans: 95.0%; (15)-Cis: 5.0%
Elemental Analysis: Calcd. (%) C: 79.18; H: 13.29; O: 7.53 Found (%) C: 79.15; H: 13.30; O: 7.55
Figure USRE037159-20010501-C00015
SYNTHESIS EXAMPLE 11 Synthesis of 1-[6(S)-2,2,6-Trimethylcyclohexan-1-yl]hexan-3-ol (16)
In a 300 ml-volume four-necked flask equipped with a condenser, a thermometer, a dropping funnel, and a stirrer were charged 5.0 g of a magnesium powder, 0.001 g of iodine, 0.5 g of n-propyl iodide, and 10 ml of tetrahydrofuran under a nitrogen atmosphere. After confirming the start of a Grignard reaction (bubbling and heat evolution), 100 ml of tetrahydrofuran was added to the reaction mixture, and 18 g of n-propyl chloride was added dropwise thereto at 35° to 40° C. over hours, followed by stirring at that temperature until the magnesium powder disappeared, to prepare a tetrahydrofuran solution of n-propylmagnesium chloride. To the resulting solution was added dropwise a solution of 15 g of the 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanal (2) obtained in Synthesis Example 5 in 15 ml of tetrahydrofuran at 5° C. over 2 hours, followed by stirring at that temperature for 4 hours to complete the reaction. The reaction mixture was worked up in a usual manner, and the resulting concentrated oil (18 g) was subjected to rectification by using a 20 cm Helipack-packed distillation column to obtain 13 g of optically active 1-[6(S)-2,2,6-trimethylcyclohexan-1-yl]hexan-3-ol (16).
Boiling point: 98°-101° C./1 mmHg
[α]D 25: +11.98°
Purity by GC: (16)-Trans: 95.2%; (16)-Cis: 4.8%
Elemental Analysis: Calcd. (%) C: 79.57; H: 13.36; O: 7.07 Found (%) C: 79.61; H: 13.33; O: 7.06
Figure USRE037159-20010501-C00016
Spectral Data of (16)-Trans:
1HNMR (400 MHz, CDCl3, δ): 0.54 (1H, m), 0.79 (3H, s), 0.87-0.95 (9H), 0.97-1.27 (3H), 1.28-1.65 (13H), 3.56 (1H, m)
MS m/e: 208 (M-18), 193 (19), 183 (11), 165 (9), 152 (13), 138 (46), 124 (61), 109 (87), 95 (65), 82 (67), 69 (100), 55 (59), 43 (17)
IR νmax (cm−1): 3340, 2958, 2920, 2870, 2840, 1466, 1460, 1387, 1378, 1368
Spectral Data of (16)-Cis:
MS m/e: 208 (17), 193 (61), 183 (4), 165 (7), 152 (8), 138 (55), 109 (93), 95 (76), 82 (81), 69 (100), 55 (61), 41 (18)
SYNTHESIS EXAMPLE 12 Synthesis of 1-[6(R)-2,2,6-Trimethylcyclohexan-1-yl]hexan-3-ol (17)
The same procedure as in Synthesis Example 11 was repeated, except for replacing 15 g of the starting 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanal with 10 g of 3-[6(R)-2,2,6-trimethylcyclohexan-1-yl]propanal, to obtain 9 g of optically active 1-[6(R)-2,2,6-trimethylcyclohexan-1-yl]hexan-3-ol (17).
Boiling point: 98°-101° C./1 mmHg
[α]D 25: 11.97°
Purity by GC: (17)-Trans: 95.1%; (17)-Cis: 4.9%
Elemental Analysis: Calcd. (%) C: 79.57; H: 13.36; O: 7.07 Found (%) C: 79.54; H: 13.37; O: 7.09
Figure USRE037159-20010501-C00017
SYNTHESIS EXAMPLE 13 Synthesis of 1-[6(S)-2,2,6-Trimethylcyclohexan-1-yl]-4-methylpentan-3-ol (18)
The same procedure as in Synthesis Example 11 was repeated; except for replacing the n-propyl iodide with isopropyl iodide and dropwise adding isopropyl chloride in place of the n-propyl chloride over 3 hours to prepare a tetrahydrofuran solution of isopropylmagnesium chloride. The resulting concentrated oil (17 g) was subjected to rectification by using a 20 cm Helipack-packed distillation column to obtain 13 g of optically active 1-[6(S)-2,2,6-trimethylcyclohexan-1-yl]-4-methylpentan-3-ol (18).
Boiling point: 96°-97° C./1 mmHg
[α]D 25: 13.71°
Purity by GC: (18)-Trans 95.1%; (18)-Cis: 4.9%
Elemental Analysis: Calcd. (%) C: 79.57; H: 13.36; O: 7.07 Found (%) C: 79.57; H: 13.36; O: 7.07
Figure USRE037159-20010501-C00018
Spectral Data of (18)-Trans:
1HNMR (400 MHz, CDCl3, δ): 0.54 (1, m), 0.79 (3H, s), 0.87-0.94 (13H), 1.00-1.70 (12H), 3.3 (1H, m)
MS m/e: 236 (M+, 4), 208 (7), 193 (7), 183 (28), 165 (10), 154 (3), 138 (22), 124 (33), 109 (73), 95 (59), 83 (67), 69 (100), 55 (33), 43 (15)
IR νmax (cm−1): 3350, 2950, 2920, 2865, 2840, 1468, 1387, 1368
Spectral Data of (18)-Cis:
MS m/e: 208 (14), 193 (36), 183 (11), 165 (8), 152 (3), 138 (33), 123 (57), 109 (74), 95 (65), 83 (77), 69 (100), 55 (35), 43 (16)
SYNTHESIS EXAMPLE 14 Synthesis of 1-[6(R)-2,2,6-Trimethylcyclohexan-1-yl]-4-methylpentan-3-ol (19)
The same procedure as in Synthesis Example 11 was repeated, except for using isopropyl iodide in place of the n-propyl iodide and adding dropwise isopropyl chloride in place of the n-propyl chloride over 3 hours to prepare a tetrahydrofuran solution of isopropylmagnesium chloride and replacing 15 g of the starting 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanal with 10 g of 3-[6(R)-2,2,6-trimethylcyclohexan-1-yl]propanal, to obtain 9 g of optically active 1-[6(R)-2,2,6-trimethylcyclohexan-1-yl]-4-methylpentan-3-ol (19).
Boiling point: 96°-97° C./1 mmHg
[α]D 25: −13.70°
Purity by GC: (19)-Trans: 95.2%; (19)-Cis: 4.8%
Elemental Analysis: Calcd. (%) C: 79.57; H: 13.36; O: 7.07 Found (%) C: 79.56; H: 13.37; O: 7.07
Figure USRE037159-20010501-C00019
SYNTHESIS EXAMPLE 15 Synthesis of 1-[6(S)-2,2,6-Trimethylcyclohexan-1-yl]heptan-3-ol (20)
The same procedure as in Synthesis Example 11 was repeated, except for using n-butyl iodide in place of the n-propyl iodide and using 20 g of n-butyl chloride in place of g of the n-propyl chloride to prepare a tetrahydrofuran solution of n-butylmagnesium chloride. The resulting concentrated oil (19 g) was subjected to rectification by using a 20 cm Helipack-packed distillation column to obtain 13 g of optically active 1-[6(S)-2,2,6-trimethylcyclohexan-1-yl]heptan-3-ol (20).
Boiling point: 109°-110° C./1 mmHg
[α]D 25: +11.23°
Purity by GC: (20)-Trans 95.2%; (20)-Cis: 4.8%
Elemental Analysis: Calcd. (%) C: 79.93; H: 13.42; O: 6.65 Found (%) C: 79.95; H: 13.41; O: 6.64
Figure USRE037159-20010501-C00020
Spectral Data of (20)-Trans:
1HNMR (400 MHz, CDCl3, δ): 0.54 (1H, m), 0.79 (3H, s), 0.88-0.93 (10H), 1.00-1.24 (2H), 1.31-1.64 (16H), 3.5 (1H, m)
MS m/e: 222 (M-18, 13), 207 (13), 183 (7), 166 (10), 154 (5), 138 (32), 124 (41), 109 (57), 95 (46), 82 (43), 69 (100), 55 (19), 41 (7)
IR νmax (cm−1): 3340, 2918, 2865, 2840, 1468, 1460 1389, 1378, 1369
Spectral Data of (20-Cis:
MS m/e: 222 (M-18, 15), 207 (50), 183 (4), 166 (4), 151 (4), 138 (36), 123 (63), 109 (63), 95 (62), 82 (56), 69 (100), 55 (22), 41 (10)
SYNTHESIS EXAMPLE 16 Synthesis of 1-[6(R)-2,2,6-Trimethylcyclohexan-1-yl]heptan-3-ol (21)
The same procedure as in Synthesis Example 11 was repeated, except for using n-butyl iodide in place of the n-propyl iodide and 20 g of n-butyl chloride in place of 18 g of the n-propyl chloride to prepare a tetrahydrofuran solution of n-butylmagnesium chloride and replacing the starting 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanal with 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanal, to obtain 9 g of optically active 1-[6(R)-2,2,6-trimethylcyclohexan-1-yl]heptan-3-ol (21).
Boiling point: 109°-110° C./1 mmHg
[α]D 25: −11.23°
Purity by GC: (21)-Trans: 95.1%; (21)-Cis: 4.9%
Elemental Analysis: Calcd. (%) C: 79.93; H: 13.42; O: 6.65 Found (%) C: 79.92; H: 13.42; O: 6.66
Figure USRE037159-20010501-C00021
SYNTHESIS EXAMPLE 17 Synthesis of 1-[6(S)-2,2,6-Trimethylcyclohexan-1-yl]-5-methylhexan-3-ol (22)
The same procedure as in Synthesis Example 11 was repeated, except for using isobutyl iodide in place of the n-propyl iodide and isobutyl chloride in place of the n-propyl chloride to prepare a tetrahydrofuran solution of isobutylmagnesium chloride. The resulting concentrated oil (18 g) was subjected to rectification by using a 20 cm Helipack-packed distillation column to obtain 13 g of optically active 1-[6(S)-2,2,6-trimethylcyclohexan-1-yl]-5-methylhexan-3-ol (22).
Boiling point: 103°-104° C./1 mmHg
[α]D 25: +10.57°
Purity by GC: (22)-Trans: 95.2%; (22)-Cis: 4.8%
Elemental Analysis: Calcd. (%) C: 79.93; H: 13.42; O: 6.65 Found (%) C: 79.91; H: 13.44; O: 6.65
Figure USRE037159-20010501-C00022
Spectral Data of (22)-Trans:
1HNMR (400 MHz, CDCl3, δ): 0.53 (1H, m), 0.79 (3H, s), 0.87-0.93 (13H), 1.00-1.65 (13H), 1.77 (1H, m), 3.6 (1H, m)
MS m/e: 222 (M-18, 9), 207 (11), 183 (11), 166 (6), 154 (7), 138 (35), 124 (37), 109 (59), 95 (44), 82 (50), 69 (100), 57 (22), 43 (15)
IR νmax (cm−1): 3350, 2950, 2920, 2865, 2840, 1468, 1387, 1368
Spectral Data of (22)-Cis:
MS m/e: 222 (M-18, 13), 207 (33), 183 (4), 166 (4), 151 (3), 138 (37), 123 (67), 109 (33), 95 (62), 69 (100), 55 (26), 43 (15)
SYNTHESIS EXAMPLE 18 Synthesis of 1-[6(R)-2,2,6-Trimethylcyclohexan-1-yl]-5-methylhexan-3-ol (23)
The same procedure as in Synthesis Example 11 was repeated, except for using isobutyl iodide in place of the n-propyl iodide and isobutyl chloride in place of the n-propyl chloride to prepare a tetrahydrofuran solution of isobutylmagnesium chloride and replacing the starting 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanal with 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanal, to obtain 9 g of optically active 1-[6(R)-2,2,6-trimethylcyclohexan-1-yl]-5-methylhexan-3-ol (23).
Boiling point: 103°-104° C./1 mmHg
[α]D 25: −10.57°
Purity by GC: (23)-Trans: 95.1%; (23)-Cis: 4.9%
Elemental Analysis: Calcd. (%) C: 79.93; H: 13.42; O: 6.65 Found (%) C: 79.93; H: 13.41; O: 6.66
Figure USRE037159-20010501-C00023
EXAMPLE 1 Odor Evaluation
Odor evaluation was carried out by a panel of 5 specialists on the 6(S)-compound, 6(R)-compound, and racemate of each of the 3-(2,2,6-trimethylcyclohexan-1-yl)propanal derivatives having various alkyl groups as R: as synthesized in the foregoing Synthesis Examples. The results are shown in Tables 1 and 2 below. Standards of rating were as follows.
A . . . Very pleasant and attractive
B . . . Pleasant and makes one to feel a desired to use
C . . . Usable but featureless
D . . . Not so interesting
E . . . Not interesting at all
TABLE 1
Com- 6(S)-Com- Com- 6(R)-Com-
pound pound Odor pound pound Odor
No. R1 Character No. Rate Character Rate
(12), CH3 slightly floral (13) B very faint E
[(13)] and orris-like woody odor
amber
fragrance
(14), C2H5 highly diffus- (15) A faint, slightly D
[(15)] ible, sharp amber-like
amber fra- woody odor
grance with with a little
slight orris- moldiness
like cam-
phorous side
note
(16), n-C3H7 highly diffus- (17) A very faint E
[(17)] ible, sharp woody odor
amber fra- with a little
grance with moldiness
slight orris-
like animal
note
(18), i-C3H7 relatively (19) C very faint E
[(19)] powerless and woody odor
slightly soil- with a little
like amber- moldiness
like woody fra-
grance
(20), n-C4H9 highly diffus- (21) A faint woody E
[(21)] ible amber odor with a
fragrance with little
slight orris- moldiness
like side note
(22), i-C4H9 highly diffus- (23) A faint woody D
[(23)] ible, sharp odor with a
amber fra- little
grance with moldiness
slight cam-
phorous side
note
TABLE 2
Racemate [Mixture of 6(S)/6(R) = 1/1]
R1 Odor Character Rate
CH3 orris-like, woody amber odor C
with a low floral side note
C2H5 low diffusible, dull, and C
orris-like woody amber odor
n-C3H7 dull and broadwise spreading B
woody amber odor
i-C3H7 faint amber odor with D
soil-like side note
n-C4H9 low diffusible, dull, and C
faint amber odor
i-C4H9 dull, broadwise spreading, and B
woody amber odor with slight
comphorous side note
EXAMPLE 2 Masking Test of Amino Acid Shampoo
In order to test masking effect on the odor of the base of an amino acid shampoo, a shampoo composition containing 1-[6(S)-2,2,6-trimethylcyclohexan-1-yl]heptane-3-ol or a racemate thereof as shown in Table 3 below was prepared, and the degree of masking was evaluated by a panel of 5 specialists. As a result, the panel judged that Composition A containing the optically active compound smelled pleasantly of amber with the base odor being perfectly masked; Composition B containing the racemate smelled considerably of the base; and the smell of the base was substantially overpowered in Composition C containing the racemate in an amount 8 times that of the optically active compound in Composition A.
TABLE 3
Composition Composition Composition
A B C
Amino acid shampoo  25 g  25 g  25 g
5% Diethylene glycol 0.1 g — —
solution of 1-[6(S)-
2,2,6-trimethylcyclo-
hexan-1-yl]heptan-3-ol
5% Diethylene glycol — 0.2 g 0.8 g
solution of racemate
[mixture of
6(S)/6(R) = 1/1]
EXAMPLE 3 Musk Base
A musk base having the following formulation was prepared, and the 1-[6(S)-2,2,6-trimethylcyclohexan-1-yl]-5-methylhexan-3-ol as synthesized in Synthesis Example 17 or a racemate thereof [mixture of 6.S()/6(R)=1/1] was compounded therein as shown in Table 4 below. Odor evaluation on the resulting perfumes (B-1, B-2), and B-4) was carried out by a panel of 5 specialists based on the following rating standards. The results are shown in Table 4. As a result of the fragrance test, the panel judged that: B-1 containing the optically active compound and B-4 containing the racemate in an amount 9 times that of the optically active compound in B-1 had an almost equal strength of fragrance, the top note of B-4 being, however, broadwise spreading and lacking sharpness, while B-1 had a well-balanced fragrance with freshness and was preferred to B-4. With respect to B-2, B-3, and B-4, the panel judged that the strength of fragrance was decreasing in the order of B-4>B-3>B-2 and that the preference was also decreasing in the same order.
Musk Base Formulation:
Coumarin  60 parts
Allyl cyclohexyloxyacetate  1 part
Hydroxycitronellal  40 parts
Geraniol  40 parts
Bourbon geranium oil  3 parts
Piperonal  20 parts
4-(4-Hydroxy-4-methylpentyl)-3-  40 parts
cyclohexenecarbaldehyde
1-Citronellal  20 parts
Linalool  20 parts
γ-Methyl isomone  40 parts
Ethylene brassylate 380 parts
10% Dipropylene glycol  8 parts
solution of 4-p-hydroxy-
phenylbutan-2-one
Phenylethyl alcohol  40 parts
Isobornylcyclohexanol 108 parts
Acetyl cedrene  80 parts
Total: 900 parts
TABLE 4
Composition Invention Comparison
(part): B-1 B-2 B-3 B-4
Musk base 900 900 900 900
1-[6(S)-2,2,6-Trimethyl-  10 — — —
cyclohexan-1-yl]-4-methyl-
hexan-3-ol
Racemate [mixture of —  20  40  90
6(S)/6(R) = 1/1]
Dipropylene glycol  90  80  60  10
Total: 100 100 100 100
Rate  5  2  3  4
Standards of Evaluation:
5 Very pleasant. Very preferable.
4 Fairly pleasant. Preferable.
3 Pleasant. Preferable.
2 Effect of addition was not so perceptible.
1 No effect of addition.
EXAMPLE 4 Perfume Composition for Detergent
A white floral perfume Composition (A) or (B) for detergents having the following formulation was prepared.
(A) (B)
Formulation: (part) (part)
7-Acetyl-1,1,3,4,4,5-hexamethyl-  50  50
1,2,3,4-tetrahydronaphthalene
Ethylene brassylate 200 200
p-Isobutyl α-methylidydro- 300 300
cinnamic aldehyde
2,4-Di-tert-butylcyclohexanone 100 100
γ-Methyl ionone  30  30
Geranium oil  10  10
Tetrahydrollinalool  50  50
Patchouli oil  10  10
Lauryl aldehyde  5  5
Methyl dihydrojasmonate 100 100
Linalool  45  45
Diethyl phthalate  90  80
1-[6(S)-2,2,6-Trimethylcyclo-  10 —
hexan-1-yl]-hexan-3-ol
Racemate [mixture of —  20
6(S)/6(R) = 1/1]
Total: 1000  1000 
Test of preference was carried out on each of Compositions (A) and (B) by a panel of 5 specialists. As a result, the panel judged that Composition (A) containing the optically active compound was better than Composition (B) because of diffusibility, freshness, and harmony of the fragrance. Further, towels were washed using each of Compositions (A) and (B), and the scent remaining on the laundry was tested by the panel. As a result, the panel judged that the towels washed by using Composition (A) had a stronger and better-balanced scent and were thus preferred.
EXAMPLE 5 Perfume Composition for Shampoo
A green floral and highly preferably perfume composition for shampoo having the following formulation was prepared.
Formulation:
Ethylene brassylate 250 parts
Musk ketone  50 parts
Methyl dihydrojasmonate  70 parts
p-Isobutyl-α-methyldihydrocinnamic 200 parts
aldehyde
1-Citronellol 100 parts
Eugenol  20 parts
2-Methyl-4-phenylbutan-2-yl acetate  50 parts
50% Dipropylene glycol solution of  10 parts
phenylacetaldehyde
2,4-Dimethyl-3-cyclohexenecarbaldehyde  10 parts
Undecylenic aldehyde  5 parts
Lime oil  20 parts
Lemon oil  40 parts
10% Dipropylene glycol  20 parts
solution of
4-p-hydroxyphenylbutan-2-one
Cis-3-hexenyl propionate  5 parts
Tetrahydrolinalool  50 parts
Benzyl salicylate  80 parts
Dipropylene glycol  10 parts
1-[6(S)-2,2,6-Trimethylcyclohexan-  10 parts
1-yl]-heptan-3-ol
Total: 1000 parts 
EXAMPLE 6 Perfume Composition for Textile Softener
A highly preferable Fougere type perfume composition for textile softeners having the following formulation was prepared.
Formulation:
Coumarin  50 parts
Ethylene brassylate 200 parts
Patchouli oil  30 parts
Dimethylbenzylmethanal 100 parts
n-Tetradecyl aldehyde  10 parts
2,4-Di-tert-butylcyclohexanone 100 parts
Benzyl salicylate 200 parts
Lavandin oil  50 parts
α-Amylcinnamic aldehyde 100 parts
Cyclamen aldehyde 100 parts
Acetylcedrene  50 parts
1-[6(S)-2,2,6-Trimethylcyclohexan-  10 parts
1-yl]-pentan-3-ol
Total: 1000 parts 
EXAMPLE 7 Perfume Composition of Soap
An aldehydic floral bouquet perfume composition (A) or (B) for soaps having he following formulation was prepared.
(A) (B)
Formulation: (part) (part)
Lauryl aldehyde 10 10
Hydroxycitronellal 50 50
Bourbon geranium oil 10 10
Piperonal 15 15
4-(4-Hydroxy-4-methylpentyl)-3- 60 60
cyclohexenecarbaldehyde
1-Citronellol 100  100 
γ-Methyl ionone 50 50
Ethylene brassylate 390  390 
Isobornylcyclohexanol 100  100 
Acetylcedrene 80 80
Patchouli oil 20 20
2,4-Dimethyl-3-cyclohexene-  5  5
carbaldhyde
Linalool 90 90
1-[6(S)-2,2,6-Trimethylcyclo- 10 —
hexan-1-yl]-4-methylhexan-3-ol
Racemate [mixture of — 20
[6(S)/6(R) = 1/1]
Dipropylene glycol 10 —
Total: 1000 parts
Evaluation test was conducted by 10 panelists on soaps perfumed with 1% of each of Compositions (A) and (B). As a result, 9 out of 10 panelists judged that the fragrance of the soap containing Composition (A) containing the optically active compound was more diffusible and deeper and therefore preferred.
EXAMPLE 8 Liquid Hypochlorite Bleachinc Agent
A liquid hypochlorite bleaching agent having the following formulation was prepared.
Formulation:
Sodium hypochlorite 40 parts
Sodium polyoxyethylene 20 parts
dodecyl ether sulfate
Sodium 2-ethylhexylsulfate 20 parts
Sodium hydroxide 10 parts
Water 10 parts
Total: 100 parts 
1-[6(S)-2,2,6-Trimethylcyclohexan-1-yl]-pentan-3-ol or a racemate thereof was added to the liquid hypochlorite bleaching solution in an amount of 0.1% or 0.2%, respectively to prepare Composition (A) or (B) having an amber fragrance.
The degree of masking of the odor of the hypochlorite in each of Compositions (A) and (B) was tested by a panel of 5 specialists. As a result, the panel judged that Composition (A) had a fresh amber-like fragrance with no perceptible odor of the hypochlorite, whereas Composition (B) smelled slightly of the hypochlorite.
Further, towels were washed in a washing machine using each of Compositions (A) and (B) as a bleaching agent, and the scent remaining on the laundry was tested by a panel of 5 specialists. As a result, the panel judged that the towels washed by using Composition (A) containing the optically active compound had a pleasant and fresh amber fragrance with no perceptible odor of the hypochlorite, whereas those washed by using Composition (B) containing the racemate smelled slightly of the hypochlorite. Incidentally, the towels washed by using Composition (A) provided bleached (whitened) to the same degree as those washed by using a bleaching agent having the same composition except for the perfume component.
The present invention provides an industrially useful optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]-propanal derivative and a perfume containing the same as an active ingredient. The optically active 3-[6(S)-2,2,6-tri-methylcyclohexan-1-yl]propanal derivative has excellent properties as a perfume, and the perfume containing the same as an active ingredient is useful in broad fields, such as various cosmetics, sanitary goods, pharmaceuticals, etc.
While the invention has been described in detail and with reference to specific embodiments thereof, it will be apparent to one skilled in the art that various changes and modifications can be made therein without departing from the spirit and scope thereof.

Claims (14)

What is claimed is:
1. An optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanol derivative represented by formula (I):
Figure USRE037159-20010501-C00024
wherein R1 represents a lower alkyl group.
2. A perfume composition comprising an optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanol derivative represented by formula (I):
Figure USRE037159-20010501-C00025
wherein R1 represents a lower alkyl group, as an active ingredient.
3. A perfume composition as in claim 2, wherein said optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]-propanol derivative represented by formula (I) is present in an amount of from 0.0001 to 50% by weight.
4. A perfume composition as in claim 3, wherein said optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanol derivative represented by formula (I) is present in an amount of from 0.001 to 20% by weight.
5. A perfume composition comprising a compound represented by formula (I) as an active ingredient, wherein 95% or more of said compound represented by formula (I) is in the trans-form:
an optically active 3-[6(S)-2,2,6-trimethyl-cyclohexan-1-yl]propanol derivative represented by formula (I):
Figure USRE037159-20010501-C00026
wherein R1 represents a lower alkyl group.
6. A perfume composition comprising a compound represented by formula (I) as an active ingredient, wherein 95% or more of said compound represented by formula (I) is in the trans form and has an optical purity of 98% ee or more:
an optically active 3-[6(S)-2,2,6-trimethyl-cyclohexane-1-yl]propanol derivative represented by formula (I):
Figure USRE037159-20010501-C00027
wherein R1 represents a lower alkyl group.
7. A perfume composition comprising a compound represented by formula (I) as an active ingredient, wherein 95% or more of said compound represented by formula 91) is in the trans form:
an optically active 3-[6(S)-2,2,6-trimethyl-cyclohexan-1-yl]propanol derivative represented by formula (I):
Figure USRE037159-20010501-C00028
wherein R1 represents an ethyl group, an n-propyl group, an n-butyl group or an isobutyl group.
8. A perfume composition comprising a compound represented by formula (I) as an active ingredient, wherein 95% or more of said compound represented by formula (I) is in the trans form and has an optical purity of 98% ee:
an optically active 3-[6(S)-2,2,6-trimethylcyclohexan-1-yl]propanol derivative represented by formula (I):
Figure USRE037159-20010501-C00029
wherein R1 represents an ethyl group, an n-propyl group, an n-butyl group or an isobutyl group.
9. A perfume composition comprising a compound represented by formula (I) as an active ingredient, wherein 95% or more of said compound represented by formula (I) is in the trans form and is obtained from 1-methoxycitronellal having an optical purity of 98% ee:
an optically active 3-[6(S)-2,2,6-trimethyl-cyclohexan-1-yl]propanol derivative represented by formula (I):
Figure USRE037159-20010501-C00030
wherein R1 represents a lower alkyl group.
10. A perfume composition comprising a mixture of two compounds represented by formula (I) as an active ingredient, wherein 95 % or more of said compounds represented by formula (I) are in the trans form with the cis form being present in an amount in combination with said 95 % or more of said trans form to impart an amber fragrance to said perfume composition, said compound represented by formula (I) having an optical purity of 98 % ee or more,
Figure USRE037159-20010501-C00031
wherein 5 % or less of said compounds represented by formula (I) are in the cis form and R 1 represents an ethyl, n-propyl, n-butyl or isobutyl group.
11. A perfume composition as claimed in claim 10, wherein the ratio of the compounds having the trans form and the compounds having the cis form ranges from 95/5-95.3/4.7 by weight.
12. The perfume composition of claim 10 wherein R1 is ethyl.
13. The perfume composition of claim 10 wherein R1 is n-propyl.
14. The perfume composition of claim 10 wherein R1 is isobutyl.
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4252896A (en) * 1980-01-07 1981-02-24 Abbott Laboratories Method of stabilizing peroxidase in a serum protein based medium
EP0118809A2 (en) * 1983-03-09 1984-09-19 Firmenich Sa Composition essentially consisting of trans-1-(2,6,6-trimethylcyclohexyl)-hexan-3-ol, utilization of same and process for its preparation; cycloaliphatic ketone and alcohol intermediates
EP0118817A1 (en) * 1983-03-11 1984-09-19 Firmenich Sa Process for the preparation of an isomeric composition of 1-(2,6,6-trimethylcyclohexyl)-hexan-3-ol, use of the obtained composition and intermediate carbinols
US4626602A (en) * 1983-04-12 1986-12-02 Firmenich Sa Aliphatic alcohols, their preparation and use of same as perfuming ingredients
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US4252896A (en) * 1980-01-07 1981-02-24 Abbott Laboratories Method of stabilizing peroxidase in a serum protein based medium
EP0118809A2 (en) * 1983-03-09 1984-09-19 Firmenich Sa Composition essentially consisting of trans-1-(2,6,6-trimethylcyclohexyl)-hexan-3-ol, utilization of same and process for its preparation; cycloaliphatic ketone and alcohol intermediates
US4623750A (en) * 1983-03-09 1986-11-18 Firmenich Sa Composition essentially consisting of trans-1-(2,6,6-trimethylcyclohexyl)-hexan-3-ol
EP0118817A1 (en) * 1983-03-11 1984-09-19 Firmenich Sa Process for the preparation of an isomeric composition of 1-(2,6,6-trimethylcyclohexyl)-hexan-3-ol, use of the obtained composition and intermediate carbinols
US4626381A (en) * 1983-03-11 1986-12-02 Firmenich Sa Process for the preparation of an isomeric mixture of 1-(2,6,6-trimethylcyclohexyl)-hexane-3-ol
US4626602A (en) * 1983-04-12 1986-12-02 Firmenich Sa Aliphatic alcohols, their preparation and use of same as perfuming ingredients
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