GB833218A - Preparation of 2, 3, 5, 6-tetrachlorobenzoyl halides and their derivatives, particularly for the production of herbicidal compositions - Google Patents
Preparation of 2, 3, 5, 6-tetrachlorobenzoyl halides and their derivatives, particularly for the production of herbicidal compositionsInfo
- Publication number
- GB833218A GB833218A GB3993/56A GB399356A GB833218A GB 833218 A GB833218 A GB 833218A GB 3993/56 A GB3993/56 A GB 3993/56A GB 399356 A GB399356 A GB 399356A GB 833218 A GB833218 A GB 833218A
- Authority
- GB
- United Kingdom
- Prior art keywords
- halide
- salt
- ester
- acid
- tetrachlorobenzoyl
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C63/00—Compounds having carboxyl groups bound to a carbon atoms of six-membered aromatic rings
- C07C63/68—Compounds having carboxyl groups bound to a carbon atoms of six-membered aromatic rings containing halogen
- C07C63/70—Monocarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/58—Preparation of carboxylic acid halides
- C07C51/62—Preparation of carboxylic acid halides by reactions not involving the carboxylic acid halide group
Abstract
2 : 3 : 5 : 6 - Tetrachlorobenzoyl halides such as the chloride and fluoride are prepared by chlorinating a benzoyl halide with chlorine in the presence of a chlorination catalyst at a temperature of 100 DEG to 230 DEG C. for a time sufficient to convert the reaction mixture at least partially into the desired product, and if desired, are converted into 2 : 3 : 5 : 6-tetrachlorobenzoic acid or a salt or ester thereof suitable by hydrolysis or reaction with an alcohol such as methanol or butanol. Suitable salts are obtained by reaction with inorganic or organic bases such as alkali or alkaline-earth metal oxides, hydroxides or carbonates, ammonia or amines such as mono-, di-or tri - alkylamines and alkanolamines. The products are used as herbicides (see Group VI).ALSO:Compositions for weed control, preventing germination, inhibiting normal growth and killing undesirable vegetation comprise as an active ingredient a 2 : 3 : 5 : 6-tetrachlorobenzyol halide such as the chloride or fluoride or a crude polychlorobenzoyl halide reaction product containing this compound, or a derivative of the halide which in the presence of water yeilds anions of 2 : 3 : 5 : 6-tetrachlorobenzoic acid, for example a salt or ester thereof (see Group IV(b)). Suitably the polychlorobenzoic acid or salt thereof such as an alkali-metal, alkaline earth metal, ammonium or amine e.g. alkylamine or alkanolamine salt, or the amide or ester is prepared in a liquid formulation in an organic solvent, optionally in the presence of a wetting or emulsifying agent, to give an emulsifiable system or in a solid or dust formulation with solid diluents, which may also contain wetting agents. Other herbicides may also be present.ALSO:Compositions for weed control, preventing germination, inhibiting growth and killing undesirable vegetation comprise as an active ingredient a 2 : 3 : 5 : 6-tetrachlorobenzoyl halide such as the chloride or fluoride or a crude polychlorobenzoyl halide reaction product containing this compound, or a derivative of the halide which in the presence of water yields anions of 2 : 3 : 5 : 6-tetrachlorobenzoic acid, for example a salt or ester thereof (see Group IV (b)). Suitably the polychlorobenzoic acid or halide, or salt thereof such as an alkali or alkaline-earth metal, ammonium or amine, e.g. alkylamine or alkanolamine, salt, or amide or ester is prepared in a liquid formulation in an organic solvent, optionally in the presence of a wetting or emulsifying agent to give an emulsifiable system or in a solid or dust formulation with solid diluents, which may also contain p wetting agents. Other herbicides may also be present.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US833218XA | 1955-04-29 | 1955-04-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB833218A true GB833218A (en) | 1960-04-21 |
Family
ID=22177577
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3993/56A Expired GB833218A (en) | 1955-04-29 | 1956-02-08 | Preparation of 2, 3, 5, 6-tetrachlorobenzoyl halides and their derivatives, particularly for the production of herbicidal compositions |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB833218A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0057844A1 (en) * | 1981-02-07 | 1982-08-18 | Bayer Ag | Process for the preparation of polychlorobenzoyl chlorides |
CN111689852A (en) * | 2020-07-23 | 2020-09-22 | 浦拉司科技(上海)有限责任公司 | Preparation method of 2,3,5, 6-tetrachlorobenzoyl chloride |
-
1956
- 1956-02-08 GB GB3993/56A patent/GB833218A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0057844A1 (en) * | 1981-02-07 | 1982-08-18 | Bayer Ag | Process for the preparation of polychlorobenzoyl chlorides |
CN111689852A (en) * | 2020-07-23 | 2020-09-22 | 浦拉司科技(上海)有限责任公司 | Preparation method of 2,3,5, 6-tetrachlorobenzoyl chloride |
CN111689852B (en) * | 2020-07-23 | 2023-01-13 | 浦拉司科技(上海)有限责任公司 | Preparation method of 2,3,5,6-tetrachlorobenzoyl chloride |
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