GB644915A - Lower alkyl esters of n-acylamino aliphatic carboxylic acids - Google Patents
Lower alkyl esters of n-acylamino aliphatic carboxylic acidsInfo
- Publication number
- GB644915A GB644915A GB15458/47A GB1545847A GB644915A GB 644915 A GB644915 A GB 644915A GB 15458/47 A GB15458/47 A GB 15458/47A GB 1545847 A GB1545847 A GB 1545847A GB 644915 A GB644915 A GB 644915A
- Authority
- GB
- United Kingdom
- Prior art keywords
- prepared
- acylamino
- sulphite
- lower alkyl
- 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
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/45—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Lower alkyl esters, i.e. methyl, ethyl and propyl esters, of N-acylamino aliphatic carboxylic acids are prepared by heating the N-acylamino acid with about one molar equivalent of dialkyl sulphite in presence of an acidic catalyst and an alcohol having the same alkyl group as the sulphite. The quantity of acid and of alcohol required is small. N-acylglycines are prepared by treating glycines with an acyl chloride. In the examples: (1) N-n-butyrylglycine is prepared from glycine and butyryl chloride and then refluxed with dimethyl sulphite in methanolic hydrogen chloride to give the methyl ester; (2) n-caproylglycine; and (3) iso-valerylglycine are both prepared and then esterified as in example (1). The Specification as open to inspection under Sect. 91 comprises a general method for the esterification of any carboxylic acid by the method above described. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US644915XA | 1946-07-13 | 1946-07-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB644915A true GB644915A (en) | 1950-10-18 |
Family
ID=22056357
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB15458/47A Expired GB644915A (en) | 1946-07-13 | 1947-06-12 | Lower alkyl esters of n-acylamino aliphatic carboxylic acids |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB644915A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3305947A (en) * | 1962-10-06 | 1967-02-28 | Kalsoy Anne Sofie Julie | Footwear with heavy sole parts |
FR2503144A1 (en) * | 1981-04-02 | 1982-10-08 | Morelle Jean | Compsns. contg. N-butyryl alpha-aminoacid(s) - for cosmetic, hygienic, therapeutic or agricultural use |
-
1947
- 1947-06-12 GB GB15458/47A patent/GB644915A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3305947A (en) * | 1962-10-06 | 1967-02-28 | Kalsoy Anne Sofie Julie | Footwear with heavy sole parts |
FR2503144A1 (en) * | 1981-04-02 | 1982-10-08 | Morelle Jean | Compsns. contg. N-butyryl alpha-aminoacid(s) - for cosmetic, hygienic, therapeutic or agricultural use |
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