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 acetamidine hydrochloride (28.8 g., 0.15 mole) and 50% sodium hydroxide (12.0 g., 0.15 mole) in 150 ml. of acetone is stirred for a period of 10 min. to liberate the free base. A solution of styrylsulfonyl chloride (10.1 g., 0.05 mole) in 50 ml. of acetone is added dropwise to the mixture at a temperature of 20°-25° C. with stirring. After further stirring for 10 min., the mixture is concentrated under reduced pressure to remove acetone, the concentrate diluted with 200 ml. of water and acidified with 3N hydrochloric acid to provide a precipitate. The precipitate is collected, dissolved in chloroform and the chloroform extract dried. Evaporation of the chloroform solvent under reduced pressure provides a white solid, m.p. 130°-134° C. which is crystallized from isopropyl acetate affording 8.5 g. (76% yield) of N-(STYRYLSULFONYL)ACETAMIDINE, m.p. 134.5°-137.0° C. (corr.).
WORKUP
后处理
- stirringAfter further stirring for 10 min.
- concentrationthe mixture is concentrated under reduced pressure
- customto remove acetone
- additionthe concentrate diluted with 200 ml
- customto provide a precipitate
- customThe precipitate is collected
- dissolutiondissolved in chloroform
- extractionthe chloroform extract
- customdried
- customEvaporation of the chloroform solvent under reduced pressure
- customprovides a white solid, m.p. 130°-134° C. which
- customis crystallized from isopropyl acetate affording 8.5 g