HRID2398461
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
5-Chloro-3-[4-(3-bromopropoxy)benzoyl]-2-phenylbenzofuran (2.0 g., 4.3 mmol.) is refluxed in 100 ml. of ethanol containing 9 ml. of diethylamine for ten hours. The reaction mixture is concentrated under reduced pressure and the residue is dissolved in ether. The ether solution is washed with aqueous sodium hydroxide and water then concentrated to give the title compound.
WORKUP
后处理
- concentrationThe reaction mixture is concentrated under reduced pressure
- dissolutionthe residue is dissolved in ether
- washThe ether solution is washed with aqueous sodium hydroxide and water
- concentrationthen concentrated