HRID217476

反应详情

EQUATION

反应方程式

HRID 217476 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

In a 2-liter flask equipped with a septum inlet, magnetic stirring bar, and condenser leading to a mercury bubbler was placed 100 g (0.348 mol) of 4-amino-3-iodobenzotrifluoride in 1 liter DMF. To this reaction flask with stirring was added 37.4 g (0.416 mol) of copper cyanide and the contents were heated to 100° C. under nitrogen for fourteen hours. Afterwards, TLC analysis revealed minor starting material (20/80) ethyl acetate/hexane. The contents were cooled to 40° C. and filtered through a pad of Celite. The solids were washed with ether and the filtrate transferred to a separatory funnel and washed with about 5% aqueous ammonium hydroxide. The aqueous layer was back-extracted with ether and the organics were combined and washed with brine, dried over magnesium sulfate, filtered and concentrated to yield a black oil. The oil was chromatographed on a Biotage 75L cartridge with ethyl acetate/hexane to obtain 68 g 2-amino-5-(trifluoromethyl)benzonitrile as a black solid.

WORKUP

后处理

  1. customIn a 2-liter flask equipped with a septum inlet, magnetic stirring bar, and condenser
  2. temperatureThe contents were cooled to 40° C.
  3. filtrationfiltered through a pad of Celite
  4. washThe solids were washed with ether
  5. customthe filtrate transferred to a separatory funnel
  6. washwashed with about 5% aqueous ammonium hydroxide
  7. extractionThe aqueous layer was back-extracted with ether
  8. washwashed with brine
  9. dry with materialdried over magnesium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated
  12. customto yield a black oil
  13. customThe oil was chromatographed on a Biotage 75L cartridge with ethyl acetate/hexane