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 20.4 g (0.1 mole) of 1-methyl-6,7-dimethoxyisoquinoline, 18.9 g (0.108 mole) of 2,6-dichlorobenzaldehyde and 15 ml of acetic anhydride is stirred in an oil bath of 150°-160° C. for 3 hours. The termination of the reaction is controlled by thin layer chromatography. The reaction mixture is cooled to a temperature between 5° C. and 10° C. under stirring, 30 ml of ether are added to it, the separated crystals are filtered and washed twice with cold ether. The thus-obtained raw product is recrystallized from a mixture of 600 ml of acetone and 130 ml of water, The clarified solution is stirred at a temperature between 0° C. and 5° C. for 2 hours, the separated substance is filtered, washed with 25 ml of a 6:1.3 mixture of 0° C. acetone and water and dried. Thus 28.4 g (79%) of 1-(2,6-dichlorostyryl)-6,7-dimethoxyisoquinoline are obtained.
WORKUP
后处理
- temperatureThe reaction mixture is cooled to a temperature between 5° C. and 10° C.
- stirringunder stirring
- filtrationthe separated crystals are filtered
- washwashed twice with cold ether
- customThe thus-obtained raw product
- customis recrystallized from a mixture of 600 ml of acetone and 130 ml of water
- stirringThe clarified solution is stirred at a temperature between 0° C. and 5° C. for 2 hours
- filtrationthe separated substance is filtered
- washwashed with 25 ml of a 6:1.3 mixture of 0° C. acetone and water
- customdried