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
1-[(4-Chlorophenyl)phenylmethyl]piperazine (573.6 mg, 2.00 mmol) and N,N-diethyl-6-chlorohexanesulfonamide (511.6 mg, 2.00 mmol) were refluxed in N-ethyldiisopropylamine (2 ml) for 6 hours. The reaction mixture was concentrated in vacuo, and water was added thereto. The mixture was extracted with chloroform. The chloroform layer was washed with water, and dried over anhydrous magnesium sulfate. Subsequently, the solvent was removed by evaporation in vacuo. The resulting crude product was purified by column chromatography on silica gel with chloroform-methanol (50:1), to give N,N-diethyl-6-[4-[(4-chlorophenyl)phenylmethyl]1-piperazinyl]hexanesulfonamide (951.0 mg) as a pale brown oil (yield: 94.0%).
WORKUP
后处理
- concentrationThe reaction mixture was concentrated in vacuo, and water
- additionwas added
- extractionThe mixture was extracted with chloroform
- washThe chloroform layer was washed with water
- dry with materialdried over anhydrous magnesium sulfate
- customSubsequently, the solvent was removed by evaporation in vacuo
- customThe resulting crude product was purified by column chromatography on silica gel with chloroform-methanol (50:1)