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
A mixture of 10.7 g (40 mmole) of 3-(2-benzoyl-4-chlorophenyl)-2-propenenitrile, 5.3 g (38 mmole) of tosylmethyl isocyanide, 75 ml of dimethyl sulfoxide and 150 ml of ether was added dropwise to a suspension of 3.7 g (77 mmole) of 50% sodium hydride in mineral oil and 170 ml of ether. When the addition was complete stirring was continued for 2 hr. The mixture was diluted with water and the ether layer was separated. The aqueous solution was extracted with ether. The combined ether extracts were washed with water, dried over anhydrous sodium sulfate; and concentrated at reduced pressure to give a dark green oil. Purification by column chromatography (800 g silica gel; eluent 5% ether in methylene chloride) gave end product as off-white prisims, mp 175°-177°.
WORKUP
后处理
- additionWhen the addition
- customthe ether layer was separated
- extractionThe aqueous solution was extracted with ether
- washThe combined ether extracts were washed with water
- dry with materialdried over anhydrous sodium sulfate
- concentrationand concentrated at reduced pressure
- customto give a dark green oil
- customPurification by column chromatography (800 g silica gel; eluent 5% ether in methylene chloride)
- customgave end product as off-white prisims, mp 175°-177°