HRID854135

反应详情

EQUATION

反应方程式

HRID 854135 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a solution of 9.0 g (50.0 mmol) of 1,4-dimethyl-5-hydroxy-3-trifluoromethyl-1H-pyrazole in 50 ml of tetrahydrofuran were added 14.4 g (55.0 mmol) of triphenylphosphine and 4.5 g (55.0 mmol) of 2,2-difluoroethanol at room temperature, followed by stirring. Furthermore, 12.3 g (60.0 mmol) of diisopropyl azodicarboxylate was added thereto under ice-cooling, followed by stirring at room temperature overnight. After the completion of the reaction was confirmed, the reaction solution was poured into water and extracted with ethyl acetate. The resulting organic layer was washed with water and saline, successively, and then dried over anhydrous magnesium sulfate. The solvent was removed by evaporation under reduced pressure and the residue was purified by silica gel column chromatography to obtain 6.8 g (yield: 55.7%) of 1,4-dimethyl-5-(2,2-difluoroethoxy)-3-trifluoromethyl-1H-pyrazole as a pale yellow liquid.

WORKUP

后处理

  1. temperatureunder ice-cooling
  2. stirringby stirring at room temperature overnight
  3. extractionextracted with ethyl acetate
  4. washThe resulting organic layer was washed with water and saline
  5. dry with materialsuccessively, and then dried over anhydrous magnesium sulfate
  6. customThe solvent was removed by evaporation under reduced pressure
  7. customthe residue was purified by silica gel column chromatography