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
14.3 ml (185 mmol) of methanesulfonyl chloride are added slowly to a solution of 15 g (84 mmol) of commercial bis(2-chloroethylamine) hydrochloride and 26 ml (185 mmol) of triethylamine in 200 ml of dichloromethane and 70 ml of tetrahydrofuran previously stirred for 15 min and then filtered in order to remove the triethylammonium chloride. The reaction medium is then stirred at ambient temperature for 18 h, extracted with dichloromethane, and washed with water. The organic phase is dried over magnesium sulfate, filtered and evaporated. The residue obtained is washed with diisopropyl ether, filtered and then dried under vacuum. 15.3 g (82%) of N,N-bis-(2-chloroethyl)methanesulfonamide are obtained in the form of a solid.
WORKUP
后处理
- filtrationfiltered in order
- customto remove the triethylammonium chloride
- stirringThe reaction medium is then stirred at ambient temperature for 18 h
- extractionextracted with dichloromethane
- washwashed with water
- dry with materialThe organic phase is dried over magnesium sulfate
- filtrationfiltered
- customevaporated
- customThe residue obtained
- washis washed with diisopropyl ether
- filtrationfiltered
- customdried under vacuum