HRID45871
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
300 mg (1.05 mmol) of 3-(3-nitrophenyl)-4-[(trimethylsilyl)ethynyl]-1H-pyrazole were suspended in 60 ml of methanol and 120 mg (2.1 mmol) of potassium fluoride were added and the mixture stirred at room temperature overnight. After this time the solvent was removed under reduced pressure and the residue taken up with dichloromethane and washed with water. The organic layer was then dried over sodium sulphate and evaporated. The crude was finally purified by flash-chromatography on a silica gel column (CH2C12-CH3COCH3 9/1), giving 150 mg (67%) of the title compound.
WORKUP
后处理
- customAfter this time the solvent was removed under reduced pressure
- washwashed with water
- dry with materialThe organic layer was then dried over sodium sulphate
- customevaporated
- customThe crude was finally purified by flash-chromatography on a silica gel column (CH2C12-CH3COCH3 9/1)