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US3131219A - Nitro and amino ketones - Google Patents

Nitro and amino ketones Download PDF

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US3131219A
US3131219A US164996A US16499662A US3131219A US 3131219 A US3131219 A US 3131219A US 164996 A US164996 A US 164996A US 16499662 A US16499662 A US 16499662A US 3131219 A US3131219 A US 3131219A
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nitro
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phenyl
useful
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US164996A
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Elkan R Blout
Myron S Simon
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Polaroid Corp
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Polaroid Corp
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    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
    • G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
    • G03C5/29—Development processes or agents therefor
    • G03C5/30—Developers
    • G03C5/3021—Developers with oxydisable hydroxyl or amine groups linked to an aromatic ring

Definitions

  • a principal object of this invention is to provide novel chemical compounds which are useful as silver halide developing agents.
  • Another object of this invention is to provide novel chemical compounds which are useful intermediates.
  • Still another object is to provide syntheses for preparing the novel compounds of this invention.
  • the invention accordingly comprises the several steps and relation and order of one or more of such steps with respect to each of the others, and the products and compositions possessing the features, properties and the relation of elements which are exemplified in the following detailed disclosure, and the scope of the application of which will be indicated in the claims.
  • novel silver halide developing agents of this invention may be represented by the formula:
  • each W is an alkoxy group, preferably a lower alkoxy group such as methoxy, ethoxy, etc., an alkyl group, preferably a lower alkyl group such as methyl, ethyl, isopropyl, etc., or a halogen such as chlorine;
  • each Z is an alkoxy group, preferably a lower alkoxy group such as methoxy, ethoxy, etc., an alkyl group, preferably a lower alkyl group such as methyl, ethyl, isopropyl, etc., a hydroxyl group, or a halogen such as chlorine;
  • m is a positive integer from 1 to 4, inclusive;
  • n is a positive integer from 1 to 5, inclusive;
  • R is an alkylene group having at least two carbon atoms, preferably a lower alkylene group such as ethylene
  • Ar is a benzene nucleus
  • R is an ethylene group
  • X is a primary amino group
  • such compounds may be represented by the formula:
  • a preferred compound within the group represented by Formula B is:
  • amino compounds of this invention may be present in the form of acid addition salts, e.g., the hydrochloride.
  • One method of preparing developing agents comprises reacting an appropriate derivative of a dihydroxyphenyl ketone, i.e., a derivat-ive which suitably protects the hydroxyl groups of said compound during reaction, e.g., a dialkoxy, a diaryloxy or a diarylalkoxy phenone derivative of said compound, with a nitro-aryl-aldehyde in the presence of an alkaline condensing Iagent, e.g., sodium, in a methanol medium, to form a compound of the formula:
  • Y is a protected dihydroXy-phenyl group, e.g., a p bis-al koxyphenyl, an o-bis-aryloxyphenyl, or a p bisaryloxyphenyl group, etc;
  • R is an unsaturated alkylene radical, e.
  • the amino group may be suitably alkylated, preferably before removing the hydroxy protective groups.
  • This product can be used directly in subsequent d'iazotization reactions.
  • the novel dihydroxyphenyl compounds of Formula A or B are useful as photographic developing agents. When used :alone, they are relatively weak. If, however, a small quantity of an accelerating developer, e.g., metol (p-methybarninophenol) or a 3- pyrazolidone, and particularly 1-phe-nyl-3-pyrazolidone, is added thereto, the combination is a very useful developing composition.
  • an accelerating developer e.g., metol (p-methybarninophenol) or a 3- pyrazolidone, and particularly 1-phe-nyl-3-pyrazolidone
  • novel class of silver halide developing agents of this invention are also useful in diiitusion-trans-fer reversal photographic processes such as disclosed in US. Patent No. 2,543,181, issued to Edwin H. Land on February 27, 1951, wherein development is effected in the presence of a silver halide solvent, e.g., sodium thiosulfate, and a suitable image-receiving layer.
  • a silver halide solvent e.g., sodium thiosulfate
  • either or both developing agents may be disposed in the photosensitive emulsion prior to the exposure of said emulsion.
  • novel compounds of this invention are also highly useful chemical intermediates. They are especially useful in reactions wherein it is desired that reaction be restrioted to the amino group.
  • novel compounds of this invention wherein X is a primary amino group
  • novel compounds of this invention are useful as intermediates in the preparation of azo compounds.
  • the novel compounds of this invention may be readily diazotized without the necessity of protecting the dihydroxyphenyl groups constituent hydroxyl radicals.
  • the compounds of this invention are particularly useful in the preparation of azo compounds, for example, as disclosed in the copending application of Elkan R. Blout, Milton Green, Howard G;
  • auxiliary developing agent may be disposed in the photosensitive element prior to the exposure of said element.
  • the novel dihydroxyphenyl compounds of this invention having an amino group may be introduced in the form of the free base or as salts thereof, such as the hydrochloride.
  • the salt may be employed where the developing agent is to be incorporated in, on or behind the silver halide emulsion or where one desires to prepare a dry developer composition, the solvent being added to the dry composition prior to use.
  • Y is a member of the group consisting of orthoand para-dihydroxyphenyl
  • W is a member of the group consisting of chlorine and lower alkyl
  • m is a positive integer from 1 to 3, inclusive, R is lower alkylene having at least two carbon atoms
  • Ar is a member of the group consisting of phenylene and naphthylene
  • Z is lower alkoxy
  • n is a positive integer from 1 to 3.
  • Y is a protected dihydroxyphenyl radical selected 9 10 from the group consisting of orthoand para-bis-alkoxy- 4. 2,5-dibenzyloxy-phenyl (2,5 dirnethoxy-3-nitro)- phenyl, bis-aryloxyphenyl and bis-aralkoxyphenyl, W is styryl ketone.

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  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

United States Patent 3,131,219 NITRO AND AMINO KETGNES Elkan R. Blout, Belmont, and Myron S. Simon, Newton Center, Mass, assignors to Polaroid Corporation, Cambridge, Mass, a corporation of Delaware No Drawing. Filed Jan. 8, 1962, Ser. No. 164,996 4 Claims. (Cl. 260-575) This invention relates to chemistry and, more particularly, to novel chemical compounds.
A principal object of this invention is to provide novel chemical compounds which are useful as silver halide developing agents.
Another object of this invention is to provide novel chemical compounds which are useful intermediates.
Still another object is to provide syntheses for preparing the novel compounds of this invention.
It is a further object of the present invention to provide novel compounds, products, developer compositions, and processes employing such novel compounds, products and developer compositions for the development of silver halide emulsions.
Other objects of this invention will in part be obvious and will in part appear hereinafter.
The invention accordingly comprises the several steps and relation and order of one or more of such steps with respect to each of the others, and the products and compositions possessing the features, properties and the relation of elements which are exemplified in the following detailed disclosure, and the scope of the application of which will be indicated in the claims.
For a fuller understanding of the nature and objects of the invention, reference should be had to the following detailed description.
The novel silver halide developing agents of this invention may be represented by the formula:
Wm-i 0 11-1 wherein Ar is an aryl nucleus, such as a benzene or naphthalene nucleus; each W is an alkoxy group, preferably a lower alkoxy group such as methoxy, ethoxy, etc., an alkyl group, preferably a lower alkyl group such as methyl, ethyl, isopropyl, etc., or a halogen such as chlorine; each Z is an alkoxy group, preferably a lower alkoxy group such as methoxy, ethoxy, etc., an alkyl group, preferably a lower alkyl group such as methyl, ethyl, isopropyl, etc., a hydroxyl group, or a halogen such as chlorine; m is a positive integer from 1 to 4, inclusive; n is a positive integer from 1 to 5, inclusive; R is an alkylene group having at least two carbon atoms, preferably a lower alkylene group such as ethylene; X is an amino group; and Y is an o-dihydroxyphenyl or a p-di hydroxyphenyl developer group. Preferably, Z is lower alkoxy, n is a positive integer from 1 to 3, inclusive, W is lower alkyl or chlorine, and m is a positive integer from 1 to 3, inclusive. 7
In a preferred embodiment, Ar is a benzene nucleus, R is an ethylene group, X is a primary amino group, and such compounds may be represented by the formula:
Zwl
3,131,219 Patented Apr. 28, 1964 "ice wherein Y, m, n, W and Z have the same meaning as above.
A preferred compound within the group represented by Formula B is:
As examples of other useful silver halide developing agents within the scope of this invention, mention may be made of the following compounds:
' Ii Q CCH2CHzCH2 NH I OH 2- [6- (4-aminophenyl) -butyryl] 'hydroquinone (3) OH 0 CH3 I H 3 I @o-cH-cm NH2 I OH 0 CH3 2L6-(2',5dimethoxy-3'-aminophenyl)-a-n1ethyl-propionyl]- hydroquinone i 2-[6- (2'-amino-pheny l -valeryl] -l1ydroqui-none II @c-cm-omG-ocn,
I on
I NH;
0 CH: II I I CCHCHZUNHZ Where desired, the amino compounds of this invention may be present in the form of acid addition salts, e.g., the hydrochloride.
One method of preparing developing agents Within the scope of this invention comprises reacting an appropriate derivative of a dihydroxyphenyl ketone, i.e., a derivat-ive which suitably protects the hydroxyl groups of said compound during reaction, e.g., a dialkoxy, a diaryloxy or a diarylalkoxy phenone derivative of said compound, with a nitro-aryl-aldehyde in the presence of an alkaline condensing Iagent, e.g., sodium, in a methanol medium, to form a compound of the formula:
(C) m-l 0 11-1 wherein W, Z, Ar, m and n have the meanings heretofore given; Y is a protected dihydroXy-phenyl group, e.g., a p bis-al koxyphenyl, an o-bis-aryloxyphenyl, or a p bisaryloxyphenyl group, etc; R is an unsaturated alkylene radical, e. g., vinylene (CH=CH) and its homologues; and X is a nitro group; and catalytically hydrogenating said compound thus saturating the double bond, reducing the nitro group and liberating the hydroxy groups, e.g., hydrogenolyzing the dibenzyloxy protective groups of said compound.
As examples of useful intermediates within the scope of Formula C, mention may be made of the following compounds:
I E I CCH=CH N02 (I) O CH:
2,5-dibenzyloxy-phenyl (2,5-dimetl1oxy-3-nit1o)-styry1 ketone 2,5-dibenzyl0xy-pl1enyl 3- 4 n itro-pheny1) -1-propenyl kehone O OCH;
CC=CH N02 (I) OCH;
2,5-dibenzyl0Xy-pl1enyl (2,5-dim'ethoxy-3-nitro-a-methy1)4 styryl ketone 2,5-diphen0Xy-phenyl 3- (4/ -nitro-pheny1)-1-etl1yl11-propeny1 ketone OCHs CHa
I O CH:
OCH3 a a C1- CC=CH- NO2 i No:
l OCHs 6-cl1lor0-2,5-dibenzyloxy-phenyl (2,5-dimetlr0xy-3-nitr0-w methyl) -styryl ketone -It is to be noted, however, that Where Ar of Formula C contains one or more 'alkoxy substituents, e.'g., methoxy, Y must be a radical such as a dibenzyloXy-phenyl radical which is cleaved by hydrogenolysis in order to form the corresponding dihydroxyphenyl developer analogue, since Y is any of the other protected dihydroxyphenyl groups, dealkylation by hydrolysis to form the dihydroxyphenyl developing function Y will also cause removal of the alkyl moiety of the alkoxy substituent on Ar of Formula C e.g., demethylation.
Where the secondary or tertiary amine derivatives are desired, the amino group may be suitably alkylated, preferably before removing the hydroxy protective groups.
The following example illustrates the preparation of 0 CH3 compounds within the scope of this invention and is given I for purposes of illustration only.
2,5-dibenzy10xy-pheny1 B (3,4-dimethoxy-6mitro-phenyl) 1- vinyl ketone Example 1 5 To prepare 2 [fl-(2',5'-dimethoXy-3'-amino-phenyl)- 5 propionyH-hydraquinone hydrochloride, 13.75 g. of 2,5- dibenzyloxyacetmphenone, 8.7 g. of 2,5-dimethoxy-3-nitro- 2 benZ-aldehyde and 0.164 g. of sodium dissolved in 15 cc. of dry methanol are mixed in approximately 600 cc. of
methanol and allowed to stand approximately 12 hours at 20 to 25 C. The mixture is then concentrated to approximately 400 cc., cooled and filtered to yield 11 g.
of 2,5-dibenzyloxy-phenyl (2,5-dimethoxy-3-nitro)-styryl 2,5-dibenzyloxy-G-mthyl-phenyl (2,5-dimeth0xy-3-nitr0-w ketone [Formula which melts at t0 C- The methyl)-styryl ketone resulting filtrate is then concentrated to approximately O f H N Calculated (percent) 70. 85 5. 1 2. 7 Found (percent) 70.5 5. 3 2. 9
10 g. of said product are dissolved in 200 cc. of glacial acetic acid by heating and hydrogenated at 34.4 p.s.i. initial pressure in the presence of 10 g. of palladiumbarium sulfate. A 9.9 p.s.i. uptake occurs in one hour. The resultant yellow filtrate is evaporated to an oil in a vacuum, dissolved in 10% hydrochloric acid, filtered, and partly evaporated. On standing 4.6 g. of khaki crystalline material, 2-[B-(2',5-dimethoxy 3' amino-phenyl)-propionylJhydroquinone hydrochloride, is precipitated, which melts at 164 to 166 C. and, when recrystallized from 10% hydrochloric acid, melts at 170 to 171 C. with decomposition.
Analysis of the product shows:
i H i N Calculated (percent) 57. 7 5. 7 4. 0 Found (percent) 58.0 5. 8 4. O
This product can be used directly in subsequent d'iazotization reactions.
As was indicated previously, the novel dihydroxyphenyl compounds of Formula A or B are useful as photographic developing agents. When used :alone, they are relatively weak. If, however, a small quantity of an accelerating developer, e.g., metol (p-methybarninophenol) or a 3- pyrazolidone, and particularly 1-phe-nyl-3-pyrazolidone, is added thereto, the combination is a very useful developing composition. As an example of a suitable photographic developer composition containing a compound of this invention and useful in conventional black-and-white tray or tank development the following is given for purposes of illustration only.
Water to make 100 cc.
The novel class of silver halide developing agents of this invention are also useful in diiitusion-trans-fer reversal photographic processes such as disclosed in US. Patent No. 2,543,181, issued to Edwin H. Land on February 27, 1951, wherein development is effected in the presence of a silver halide solvent, e.g., sodium thiosulfate, and a suitable image-receiving layer.
It will be apparent that the relative proportions of the novel agents of the developer composition set forth above may be varied to suit the requirements of the operator. Thus it is within the scope of this invention to modify said developing composition by the substitution of preservatives, alkalies, silver halide solvents, etc., other than those specifically mentioned. It is also contemplated that where desirable the said developer composition may be modified by the inclusion of other common components of developer compositions such as restrainers, accelerators, etc. Similarly, the concentration of the developing agent may be varied over a wide range and, where desirable,
either or both developing agents may be disposed in the photosensitive emulsion prior to the exposure of said emulsion.
The novel compounds of this invention are also highly useful chemical intermediates. They are especially useful in reactions wherein it is desired that reaction be restrioted to the amino group.
In particular, the novel compounds of this invention, wherein X is a primary amino group, are useful as intermediates in the preparation of azo compounds. In the past it has been generally accepted that it is substantially impossible to diazotize a primary amino compound in the presence of a free hydroquinone group. However, it has been discovered that the novel compounds of this invention may be readily diazotized without the necessity of protecting the dihydroxyphenyl groups constituent hydroxyl radicals. Thus, the compounds of this invention are particularly useful in the preparation of azo compounds, for example, as disclosed in the copending application of Elkan R. Blout, Milton Green, Howard G;
Rogers and Myron S. Simon, Serial No. 685,081, filed September 20, 1957.
The presence of the acyl group, i.e., the
hydroquinone, metol, amidol, benzylaminophenol, or a 3-pyrazolidone, such as 1-phenyl-3-pyrazolidone, etc. It will be apparent that the desired auxiliary developing agent may be disposed in the photosensitive element prior to the exposure of said element.
When employed as photographic developing agents, the novel dihydroxyphenyl compounds of this invention having an amino group may be introduced in the form of the free base or as salts thereof, such as the hydrochloride. Thus, the salt may be employed where the developing agent is to be incorporated in, on or behind the silver halide emulsion or where one desires to prepare a dry developer composition, the solvent being added to the dry composition prior to use.
This application is a continuation-in-part of copending application Serial No. 685,066, filed September 20, 1957, now abandoned.
Since certain changes may be made in the above processes, products and compositions without departing from the scope of the invention herein involved, it is intended that all matter contained in the above description shall be interpreted as illustrative and not in a limiting sense.
What is claimed is:
1. A compound of the formula:
wherein Y is a member of the group consisting of orthoand para-dihydroxyphenyl; W is a member of the group consisting of chlorine and lower alkyl; m is a positive integer from 1 to 3, inclusive, R is lower alkylene having at least two carbon atoms; Ar is a member of the group consisting of phenylene and naphthylene; Z is lower alkoxy; and n is a positive integer from 1 to 3.
2. 2 [,8 (2'5 dimethoxy 3 amino-phenyl) propionyl] -hydroquinone.
3. A compound of the formula:
wherein Y is a protected dihydroxyphenyl radical selected 9 10 from the group consisting of orthoand para-bis-alkoxy- 4. 2,5-dibenzyloxy-phenyl (2,5 dirnethoxy-3-nitro)- phenyl, bis-aryloxyphenyl and bis-aralkoxyphenyl, W is styryl ketone. a member of the group consisting of chlorine and lower References Cited in the file of this Patent alkyl; m is a positive integer from 1 to 3 inclusive; R is divalent alkene; Ar is a member of the group consist- 5 UNITED STATES PATENTS ing of phenylene and naphthylene; Z is lower alkoxy; 2,769,817 Martin et a1 Nov. 6, 1956 and n is a positive integer from 1 to 3. 3,062,884 Green Nov. 6, 1962 UNITED STA ES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3,13i,219 April 28 1964 Elkan R. Blout et al., I
It is hereby certified that error appears in the above numbered patent requiring correction and that the said Letters Patent should read as corrected below.
Column 1, line 38, for "(V)" read (A) column 2, line 13, for propionyll" read -propionyl line 27 for ".6 read b same column 2, line 65, for "-phenyDpropionyl" read phenyD-propionyl column 7 line 21, for "pionyl] hydroquinone" read pionylj hydroquinone Signed and sealed this 3rd day of November 1964,
(SEAL) Attest:
ERNEST W. SWIDER EDWARD J. BRENNER Altosting Officer I Commissioner of Patents

Claims (1)

1. A COMPOUND OF THE FORMULA:
US164996A 1962-01-08 1962-01-08 Nitro and amino ketones Expired - Lifetime US3131219A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3789062A (en) * 1968-02-19 1974-01-29 Polaroid Corp Ligands which are also silver halide developing agents

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2769817A (en) * 1951-06-07 1956-11-06 Nat Drug Co Therapeutic substituted chalcones
US3062884A (en) * 1955-06-08 1962-11-06 Polaroid Corp Catalytic hydrogenation of 2, 5-dialkoxy-beta-nitrostyrene to produce beta-aminoethylhydroquinone

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2769817A (en) * 1951-06-07 1956-11-06 Nat Drug Co Therapeutic substituted chalcones
US3062884A (en) * 1955-06-08 1962-11-06 Polaroid Corp Catalytic hydrogenation of 2, 5-dialkoxy-beta-nitrostyrene to produce beta-aminoethylhydroquinone

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3789062A (en) * 1968-02-19 1974-01-29 Polaroid Corp Ligands which are also silver halide developing agents

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