GB636333A - Improvements in and relating to the manufacture of aromatic amino carboxylic acids - Google Patents

Improvements in and relating to the manufacture of aromatic amino carboxylic acids

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Publication number
GB636333A
GB636333A GB523247A GB523247A GB636333A GB 636333 A GB636333 A GB 636333A GB 523247 A GB523247 A GB 523247A GB 523247 A GB523247 A GB 523247A GB 636333 A GB636333 A GB 636333A
Authority
GB
United Kingdom
Prior art keywords
carbon dioxide
alkali metal
bicarbonate
acid
amino
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
Application number
GB523247A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
DAVID DUNCANSON MARTIN
Smith and Nephew Nominee Services Ltd
Original Assignee
DAVID DUNCANSON MARTIN
Herts Pharmaceuticals Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by DAVID DUNCANSON MARTIN, Herts Pharmaceuticals Ltd filed Critical DAVID DUNCANSON MARTIN
Priority to GB523247A priority Critical patent/GB636333A/en
Publication of GB636333A publication Critical patent/GB636333A/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Alkali metal salts of 4-amino-2-hydroxy benzoic acid are prepared by the reaction of carbon dioxide with m-aminophenol in the presence of an alkali metal hydroxide, carbonate or p bicarbonate and water, preferably at a temperature of over 100 DEG C. Conveniently, the reaction may be carried out by heating m-amino phenol with the alkali-metal compound and solid carbon dioxide in an autoclave at about 130 DEG C. The free acid may be liberated from the reaction product by adding dilute hydrochloric acid until just acid to litmus, or by dissolving in an excess of hydrochloric acid to form the aminoacid hydrochloride which is separated and dried and treated with an equivalent quantity of an alkali metal bicarbonate and just sufficient water to dissolve the alkali metal chloride formed. In examples: (1) m-aminophenol, potassium bicarbonate, solid carbon dioxide and water are heated in an autoclave and the reaction product is neutralized with hydrochloric acid to give 4-amino-2-hydroxy benzoic acid; (2) sodium bicarbonate is used in place of potassium bicarbonate in (1) and (3), the process (1) is repeated using gaseous carbon dioxide in place of solid carbon dioxide and the product is separated by means of the aminoacid hydrochloride. Reference has been directed by the Comptroller to Berichte der Deutschen Chemischen Gesellschaft (Referat), Volume 23 (1890), page 313.
GB523247A 1947-02-22 1947-02-22 Improvements in and relating to the manufacture of aromatic amino carboxylic acids Expired GB636333A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB523247A GB636333A (en) 1947-02-22 1947-02-22 Improvements in and relating to the manufacture of aromatic amino carboxylic acids

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB523247A GB636333A (en) 1947-02-22 1947-02-22 Improvements in and relating to the manufacture of aromatic amino carboxylic acids

Publications (1)

Publication Number Publication Date
GB636333A true GB636333A (en) 1950-04-26

Family

ID=9792193

Family Applications (1)

Application Number Title Priority Date Filing Date
GB523247A Expired GB636333A (en) 1947-02-22 1947-02-22 Improvements in and relating to the manufacture of aromatic amino carboxylic acids

Country Status (1)

Country Link
GB (1) GB636333A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2700669A (en) * 1951-09-27 1955-01-25 American Cyanamid Co Hydroxybenzotriazole carboxylic acids
DK85717C (en) * 1950-06-24 1958-06-16 Smith & Nephew Process for the preparation of p-amino-salicylic acid or salts thereof.

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK85717C (en) * 1950-06-24 1958-06-16 Smith & Nephew Process for the preparation of p-amino-salicylic acid or salts thereof.
US2700669A (en) * 1951-09-27 1955-01-25 American Cyanamid Co Hydroxybenzotriazole carboxylic acids

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