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3-chloro-N-(2-chlorophenyl)benzamide synthesis

2synthesis methods
-

Yield:83426-46-4 90.2%

Reaction Conditions:

with pyridine for 2 h;Reflux;

Steps:



General procedure: A mixture of 0.53 ml (5 mmol) 2-cloroaniline, 0,58 mlbenzoyl chloride (5 mmol) and 5 ml of pyridine in a 50 mlround bottomed flask was refluxed for 2 hrs. After cooled toroom temperature, the reaction mixture was poured into 200ml of cold water and 5 ml of HCl 10% solution. The precipitateswere filtered, washed with water and dried at 60-70°C to give a crude product. Recrystallization from n-hexane/acetone furnished 1.01g of 2a.

References:

Nam, Nguyen Hai;Dung, Phan Thi Phuong;Thuong, Phuong Thien [Medicinal Chemistry,2011,vol. 7,# 2,p. 127 - 134]