HRID53103

反应详情

EQUATION

反应方程式

HRID 53103 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

2-Amino-5-bromobenzonitrile (3.94 g, 20 millimoles), triethylamine (2.22 g, 22 millimoles) and 4-dimethylamino- pyridine (0.49 g, 4 millimoles) were dissolved in 40 ml of dry dichloromethane, to which was slowly added dropwise a solution of 4-diethoxyphosphinoylmethylbenzoyl chloride (5.81 g, 20 millimoles) in 40 ml dry dichloromethane while cooling the system with ice and stirring it. After stirring the resulting mixture at ambient temperature for 10 hours, the reaction mixture was mixed with 50 ml of water and extracted with chloroform. The chloroform layer was dried on anhydrous sodium sulfate and the solvent was removed by evaporation under reduced pressure. Purification of the residue by a silica gel column chromato-graphy using 1:2 mixture of chloroform and ethyl acetate as an eluent, followed by recrystallization from benzene-n-hexane mixture, gave 2.94 g of 4-diethoxyphosphinoylmethyl-N-(4-bromo-2-cyanophenyl)benzamide as a colorless crystalline product melting at 165°-166° C. (after recrystallization from benzene-n-hexane).

WORKUP

后处理

  1. temperaturewhile cooling the system with ice
  2. stirringAfter stirring the resulting mixture at ambient temperature for 10 hours
  3. extractionextracted with chloroform
  4. dry with materialThe chloroform layer was dried on anhydrous sodium sulfate
  5. customthe solvent was removed by evaporation under reduced pressure
  6. customPurification of the residue by a silica gel column chromato-graphy
  7. addition1:2 mixture of chloroform and ethyl acetate as an eluent
  8. customfollowed by recrystallization from benzene-n-hexane mixture