HRID13484

反应详情

EQUATION

反应方程式

HRID 13484 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

A solution of 5-fluoro-2-nitrophenylamine (1 eq) in methylenechloride was treated with trifluoroacetic anhydride (1 eq) and stirred for 10 minutes at 0° C. The mixture was quenched with saturated sodium bicarbonate solution. The organic layer was separated and washed with water, brine, dried and evaporated. To the solution of the trifluoroacetamide (1 eq) in a mixture of toluene, acetonitrile and sodium hydroxide solution (50%) was added benzyltrimethylammonium chloride (1 eq) and dimethyl sulfate (1.2 eq). The biphasic mixture was stirred overnight at room temperature and evaporated. The mixture was taken up in ethyl acetate, washed with water, brine, dried and evaporated. The crude was purified by column chromatography eluting with 1:1 hexanes and ethyl acetate to afford (5-fluoro-2-nitrophenyl)methylamine. MS: MH+=170.

WORKUP

后处理

  1. customThe mixture was quenched with saturated sodium bicarbonate solution
  2. customThe organic layer was separated
  3. washwashed with water, brine
  4. customdried
  5. customevaporated
  6. stirringThe biphasic mixture was stirred overnight at room temperature
  7. customevaporated
  8. washwashed with water, brine
  9. customdried
  10. customevaporated
  11. customThe crude was purified by column chromatography
  12. washeluting with 1:1 hexanes and ethyl acetate