GB834814A - ª‡-substituted o, o-dialkyl-dithiophosphorylacetic esters and process for their preparation - Google Patents
ª‡-substituted o, o-dialkyl-dithiophosphorylacetic esters and process for their preparationInfo
- Publication number
- GB834814A GB834814A GB17434/56A GB1743456A GB834814A GB 834814 A GB834814 A GB 834814A GB 17434/56 A GB17434/56 A GB 17434/56A GB 1743456 A GB1743456 A GB 1743456A GB 834814 A GB834814 A GB 834814A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ethyl
- dithiophosphoryl
- diethyl
- acetone
- acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/1651—Esters of thiophosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
The invention comprises O,O-dialkyl-dithiophosphorylacetic esters of the general formula <FORM:0834814/IV (b)/1> (wherein R4, R5 and R6 are like or different, saturated or unsaturated, straight- or branchedchain alkyl radicals and R3 is a substituted or unsubstituted aryl radical). They are prepared by reacting a salt of an O,O-dialkyl-dithiophosphoric ester <FORM:0834814/IV (b)/2> (wherein Y is ammonium, alkali metal or alkaline-earth metal) with an a -halogeno-a -arylacetic ester <FORM:0834814/IV (b)/3> (wherein Z is Cl, Br or I) in the presence of a solvent for either or both reactants. The salt may be prepared in situ by neutralizing the free acid. Suitable solvents are water, alcohols, ketones, esters, dioxane or aromatic hydrocarbons. The reaction may be effected at room temperature or under reflux. The products have insecticidal activity. In examples, the following esters are prepared, the free dialkyl-di-thiophosphoric acid being first neutralized with anhydrous sodium carbonate in each case; (1) ethyl O,O-diethyl-dithiophosphoryl-phenylacetate from O,O-diethyl-dithiophosphoric acid and ethyl a -phenyl-a -bromoacetate in acetone solution; (2) ethyl O,O-diethyl - dithiophosphoryl - p - nitrophenylacetate from O,O-diethyl-dithiophosphoric acid and ethyl a - p - nitrophenyl - a - bromoacetate in acetone; (3) ethyl O,O-dimethyl-dithiophosphoryl - phenylacetate from O,O - dimethyldithiophosphoric acid and ethyl a -phenyl-a -bromoacetate in acetone; (4) ethyl O,O-diisopropyl - dithiophosphoryl - phenylacetate from O,O - diisopropyl - dithiophosphoric acid and ethyl a - phenyl - a - bromoacetate in acetone; (5) ethyl O,O - diethyl - dithiophosphoryl - p - chlorophenylacetate from O,O-diethyl-dithiophosphoric acid and ethyl p-chlorophenyl-a -chloroacetate in acetone; (6) ethyl O,O-diisopropyl-dithiophosphoryl-p-chlorophenylacetate from O,O - diisopropyl - dithiophosphoric acid and ethyl a -p-chlorophenyl-a -chloroacetate in acetone; (7) isopropyl O,O-diethyl-dithiophosphoryl-phenylacetate from O,O-diethyl-dithiophosphoric acid and isopropyl a -phenyl-a -bromoacetate in ethyl alcohol; (8) methyl O,O - dimethyl - dithiophosphoryl - phenylacetate from O,O-dimethyl-dithiophosphoric acid and methyl a -phenyl-a -bromoacetate in dioxane; (9) ethyl O,O-diisopropyl-dithiophosphoryl-naphthylacetate from O,O-diisopropyldithiophosphoric acid and ethyl a -naphthyl-a -chloroacetate in acetone. Reference has been directed by the Comptroller to Specification 803,441.ALSO:Pesticidal compositions comprise O,O-dialkyldithiophosphorylacetic esters of formula <FORM:0834814/VI/1> wherein R4, R5 and R6 are like or unlike, saturated or unsaturated, straight- or branched-chain alkyl radicals and R3 is a substituted or unsubstituted aryl radical. (For preparation see Group IV (b)). Other disinfecting compounds and/or plant nutrients and/or fertilizers may be present. Aqueous dispersions and acetone and benzene solutions are used in examples. Reference has been directed by the Comptroller to Specification 803,441.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT834814X | 1955-06-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB834814A true GB834814A (en) | 1960-05-11 |
Family
ID=11322444
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB17434/56A Expired GB834814A (en) | 1955-06-14 | 1956-06-06 | ª‡-substituted o, o-dialkyl-dithiophosphorylacetic esters and process for their preparation |
Country Status (3)
| Country | Link |
|---|---|
| CY (1) | CY239A (en) |
| GB (1) | GB834814A (en) |
| MY (1) | MY6200030A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6818670B2 (en) | 1999-11-09 | 2004-11-16 | Bayer Aktiengesellschaft | Active ingredient combination having insecticidal and acaricidal characteristics |
| US6900190B2 (en) | 2000-03-28 | 2005-05-31 | Bayer Aktiengesellschaft | Active substance combinations having insecticidal and acaricidal properties |
| US7060692B2 (en) | 2000-08-31 | 2006-06-13 | Bayer Cropscience Ag | Active ingredient combinations comprising insecticidal and acaricidal properties |
| DE102007045955A1 (en) | 2007-09-26 | 2009-04-09 | Bayer Cropscience Ag | Active agent combination, useful e.g. for combating animal pests and treating seeds of transgenic plants, comprises substituted amino-furan-2-one compound and at least one compound e.g. diazinon, isoxathion, carbofuran or aldicarb |
| US7560445B2 (en) | 2005-07-06 | 2009-07-14 | Taro Pharmaceuticals North America, Inc. | Process for preparing malathion for pharmaceutical use |
| US8012498B2 (en) | 2004-07-12 | 2011-09-06 | Sandhya Goyal | Topical gel formulation comprising organophosphate insecticide and preparation thereof |
| US8158139B2 (en) | 2004-07-12 | 2012-04-17 | Taro Pharmaceuticals North America, Inc. | Topical gel formulation comprising organophosphate insecticide and preparation thereof |
| US8846567B2 (en) | 2009-03-25 | 2014-09-30 | Bayer Cropscience Ag | Active compound combinations having insecticidal and acaricidal properties |
-
1956
- 1956-06-06 GB GB17434/56A patent/GB834814A/en not_active Expired
-
1962
- 1962-03-15 CY CY23962A patent/CY239A/en unknown
- 1962-12-31 MY MY6200030A patent/MY6200030A/en unknown
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6818670B2 (en) | 1999-11-09 | 2004-11-16 | Bayer Aktiengesellschaft | Active ingredient combination having insecticidal and acaricidal characteristics |
| US6900190B2 (en) | 2000-03-28 | 2005-05-31 | Bayer Aktiengesellschaft | Active substance combinations having insecticidal and acaricidal properties |
| US7060692B2 (en) | 2000-08-31 | 2006-06-13 | Bayer Cropscience Ag | Active ingredient combinations comprising insecticidal and acaricidal properties |
| US8012498B2 (en) | 2004-07-12 | 2011-09-06 | Sandhya Goyal | Topical gel formulation comprising organophosphate insecticide and preparation thereof |
| US8158139B2 (en) | 2004-07-12 | 2012-04-17 | Taro Pharmaceuticals North America, Inc. | Topical gel formulation comprising organophosphate insecticide and preparation thereof |
| US7560445B2 (en) | 2005-07-06 | 2009-07-14 | Taro Pharmaceuticals North America, Inc. | Process for preparing malathion for pharmaceutical use |
| US7977324B2 (en) | 2005-07-06 | 2011-07-12 | Taro Pharmaceuticals North America, Inc. | Process for preparing malathion for pharmaceutical use |
| US8039657B2 (en) | 2005-07-06 | 2011-10-18 | Taro Pharmaceuticals North America, Inc. | Process for preparing malathion for pharmaceutical use |
| US8536155B2 (en) | 2005-07-06 | 2013-09-17 | Taro Pharmaceuticals North America, Inc. | Process for preparing malathion for pharmaceutical use |
| US8957238B2 (en) | 2005-07-06 | 2015-02-17 | Taro Pharmaceuticals North America, Inc. | Process for preparing malathion for pharmaceutical use |
| DE102007045955A1 (en) | 2007-09-26 | 2009-04-09 | Bayer Cropscience Ag | Active agent combination, useful e.g. for combating animal pests and treating seeds of transgenic plants, comprises substituted amino-furan-2-one compound and at least one compound e.g. diazinon, isoxathion, carbofuran or aldicarb |
| US8846567B2 (en) | 2009-03-25 | 2014-09-30 | Bayer Cropscience Ag | Active compound combinations having insecticidal and acaricidal properties |
Also Published As
| Publication number | Publication date |
|---|---|
| MY6200030A (en) | 1962-12-31 |
| CY239A (en) | 1962-03-15 |
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