GB607113A - Improvements relating to the manufacture of halogenated carboxylic acids - Google Patents
Improvements relating to the manufacture of halogenated carboxylic acidsInfo
- Publication number
- GB607113A GB607113A GB788346A GB788346A GB607113A GB 607113 A GB607113 A GB 607113A GB 788346 A GB788346 A GB 788346A GB 788346 A GB788346 A GB 788346A GB 607113 A GB607113 A GB 607113A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- prepared
- glacial acetic
- chlorine
- carboxylic acids
- 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
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/64—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
- C07C59/66—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings
- C07C59/68—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings the oxygen atom of the ether group being bound to a non-condensed six-membered aromatic ring
- C07C59/70—Ethers of hydroxy-acetic acid, e.g. substitutes on the ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
- C07C51/363—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by introduction of halogen; by substitution of halogen atoms by other halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/64—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
- C07C59/66—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings
- C07C59/68—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings the oxygen atom of the ether group being bound to a non-condensed six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Mono-, di- or tri-nuclear chlorinated phenoxyalkyl carboxylic acids are prepared by chlorinating the corresponding carboxylic acid in a solvent at an elevated temperature. Specified solvents are glacial acetic acid and tetrachlorethylene. The degree of substitution is controlled by using substantially the theoretical amount of chlorine to produce the required compound. The progress of the chlorination is preferably followed by determination of the amount of evolved hydrochloric acid. In examples: (1) chlorine is passed into a solution of phenoxyacetic acid in glacial acetic acid giving 4-chlorophenoxyacetic acid; (2) 2 : 4-dichlorophenoxyacetic acid is similarly prepared; (3) 2 : 4 : 6-trichlorophenoxyacetic acid is similarly prepared; (4) 2 : 4-dichloro-g -phenoxybutyric acid is prepared from g -phenoxybutyric acid by chlorination as in (1) in the presence of a trace of iodine, and (5) 2 : 4-dichloro-a -phenoxypropionic acid is prepared by passing chlorine into a solution of a -phenoxypropionic acid in glacial acetic acid in the presence of a reduced iron powder catalyst.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB788346A GB607113A (en) | 1946-03-13 | 1946-03-13 | Improvements relating to the manufacture of halogenated carboxylic acids |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB788346A GB607113A (en) | 1946-03-13 | 1946-03-13 | Improvements relating to the manufacture of halogenated carboxylic acids |
Publications (1)
Publication Number | Publication Date |
---|---|
GB607113A true GB607113A (en) | 1948-08-25 |
Family
ID=9841623
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB788346A Expired GB607113A (en) | 1946-03-13 | 1946-03-13 | Improvements relating to the manufacture of halogenated carboxylic acids |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB607113A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2796427A (en) * | 1952-05-14 | 1957-06-18 | Philips Corp | Method of producing 2, 4, 5, trichlorophenoxyalkanecarboxylic acids or esters thereof |
US2811547A (en) * | 1957-10-29 | Process for preparing s-chlorosalicylic | ||
DE1035152B (en) * | 1954-05-04 | 1958-07-31 | Diamond Alkali Co | Process for the preparation of 2-methyl-4-chlorophenoxyacetic acid |
US3331869A (en) * | 1963-07-18 | 1967-07-18 | Frederick Post Co | Halogenated phloroglucinol carboxylic acid |
EP0509518A1 (en) * | 1991-04-16 | 1992-10-21 | ENICHEM AGRICOLTURA S.p.A. | Process for the preparation of 2,4-dichlorophenoxyacetic acid |
CN113979860A (en) * | 2021-11-11 | 2022-01-28 | 天津大学 | 2, 4-dichlorophenoxyacetic acid crystal and preparation method and application thereof |
-
1946
- 1946-03-13 GB GB788346A patent/GB607113A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2811547A (en) * | 1957-10-29 | Process for preparing s-chlorosalicylic | ||
US2796427A (en) * | 1952-05-14 | 1957-06-18 | Philips Corp | Method of producing 2, 4, 5, trichlorophenoxyalkanecarboxylic acids or esters thereof |
DE1035152B (en) * | 1954-05-04 | 1958-07-31 | Diamond Alkali Co | Process for the preparation of 2-methyl-4-chlorophenoxyacetic acid |
US3331869A (en) * | 1963-07-18 | 1967-07-18 | Frederick Post Co | Halogenated phloroglucinol carboxylic acid |
EP0509518A1 (en) * | 1991-04-16 | 1992-10-21 | ENICHEM AGRICOLTURA S.p.A. | Process for the preparation of 2,4-dichlorophenoxyacetic acid |
CN113979860A (en) * | 2021-11-11 | 2022-01-28 | 天津大学 | 2, 4-dichlorophenoxyacetic acid crystal and preparation method and application thereof |
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