HRID1979562
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 3.5 g (10 mmole) of 1-(2-chlorophenyl)-3,4-dihydro-4-[(dimethylamino)methylene]-5H-2-benzazepin-5-one, 4.8 g (40 mmole) of isobutyramidine hydrochloride, 10 ml (41 mmole) of a 4.12 M methanol solution of sodium methoxide and 100 ml of methanol was stirred at room temperature for 2 hr. The mixture was diluted with water and extracted with methylene chloride. The methylene chloride solution was dried over anhydrous sodium sulfate and concentrated at reduced pressure to give a yellow oil. Crystallization of the oil with ether gave a light yellow solid, mp 127°-129° C. Recrystallization from a mixture of ether and petroleum ether gave colorless rods, mp 127°-129° C.
WORKUP
后处理
- extractionextracted with methylene chloride
- dry with materialThe methylene chloride solution was dried over anhydrous sodium sulfate
- concentrationconcentrated at reduced pressure
- customto give a yellow oil
- customCrystallization of the oil with ether
- customgave a light yellow solid, mp 127°-129° C
- customRecrystallization
- additionfrom a mixture of ether and petroleum ether
- customgave colorless rods, mp 127°-129° C.