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70547-29-4

ETHYL 4-HYDROXY-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLATE synthesis

3synthesis methods
-

Yield:70547-29-4 88%

Reaction Conditions:

in ethanol; for 2 h;Heating / reflux;

Steps:

6.1

Reference Example 6; 4-methoxy-2-phenyl-l , 3-thiazole-5-carbaldehγde; (step 1); A solution of benzenecarbothioamide (50 g) and diethyl bromomalonate (95.6 g) in ethanol (350 mL) was refluxed with heating for 2 hrs, and the mixture was cooled to room temperature. The precipitate was filtrated with cold ethanol. The filtrate was concentrated and the precipitate was filtrated with cold ethanol . This operation was done twice to give ethyl 4-hydroxy-2-phenyl-l, 3-thiazole-5-carboxylate (79.8 g, 88%) as pale-yellow crystals.

References:

WO2007/89031,2007,A1 Location in patent:Page/Page column 88