HRID2116686

反应详情

EQUATION

反应方程式

HRID 2116686 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

Under protective nitrogen gas 2.02 g (9.0 mmol) palladium(II)acetate and 2.82 g (9.0 mmol) tri-o-tolylphosphine were added to a mixture of 25.0 g (113 mmol) 4-bromo-2-chloro-6-methyl-aniline, 19.9 g (136 mmol) methyl 2-acetamidoacrylate, 350 ml triethylamine and 150 ml acetonitrile at ambient temperature. The reaction mixture was stirred for 18 hours at 80° C., evaporated down under reduced pressure, the residue was combined with 600 ml dichloromethane and water and filtered off from the insoluble precipitate. The organic phase was dried over sodium sulphate, evaporated down under reduced pressure and then combined with 200 ml of ethyl acetate/cyclohexane (3/1). The insoluble fraction was suction filtered and the mother liquor was purified by column chromatography through silica gel. The corresponding fractions were evaporated down under reduced pressure and combined with the insolublen fraction suction filtered previously.

WORKUP

后处理

  1. customevaporated down under reduced pressure
  2. filtrationfiltered off from the insoluble precipitate
  3. dry with materialThe organic phase was dried over sodium sulphate
  4. customevaporated down under reduced pressure
  5. filtrationfiltered
  6. customthe mother liquor was purified by column chromatography through silica gel
  7. customThe corresponding fractions were evaporated down under reduced pressure
  8. filtrationfiltered previously