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    • 2. 发明专利
    • Improvements in and relating to the manufacture of aromatic amino carboxylic acids
    • GB636333A
    • 1950-04-26
    • GB523247
    • 1947-02-22
    • HERTS PHARMACEUTICALS LTDDAVID DUNCANSON MARTINDONALD EDWIN SEYMOURFRANK STUART SPRING
    • 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.