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ChemicalBook CAS DataBase List Oxaprozin
21256-18-8

Oxaprozin synthesis

6synthesis methods
-

Yield:21256-18-8 67%

Reaction Conditions:

with pyridine;ammonium acetate in water;acetic acid

Steps:

1 EXAMPLE 1
EXAMPLE 1 A 5 liter flask was set up and equipped with stirrer, thermometer, reflux condenser and nitrogen inlet. Succinic anhydride (373 grams), benzoin (531 grams) and pyridine (300 milliliters; 296 grams) were introduced. The flask was purged with nitrogen and the reaction mixture heated to 90°-95° C. The mixture was stirred for one and a half hours at this temperature. Glacial acetic acid (1300 milliliters) and ammonium acetate (385 grams) were added to the reaction mixture and the mixture reheated to 90°-95° C. Stirring was continued and this temperature was maintained for a further 2 hours. The mixture was filtered, rinsing through with glacial acetic acid (150 milliliters). Distilled water (750 milliliters) was added and the mixture reheated to 90°-95° C. before gradual cooling with stirring to 15° C. over 1 hour. After filtering and washing with a mixture of acetic acid and distilled water in a ratio of 2:1 (600 milliliters), the product was slurried with distilled water (1000 milliliters). After filtering and washing with distilled water (2*400 milliliters), the product was dried at 90°-100° C. under vacuum. 702 Grams (67% yield) of β-(4,5-diphenyloxazol-2-yl)propionic acid were obtained as a white crystalline powder, m.p. 163°-165° C. The material was investigated for quality by TLC. The product had high purity and merely showed a number of very faint trace impurities.

References:

John Wyeth & Brother Limited US4190584, 1980, A

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