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 suspension of 103 g. of 2,6-dimethoxy-4-(methoxy-carbonyl)-carbanilic acid benzyl ester and 17.3 g. of sodium hydride (50% dispersion in oil) in 1 liter of absolute dimethylformamide was stirred at room temperature for 4 hours and subsequently treated with 56.2 g. of ethyl iodide with stirring and ice-cooling. After stirring at room temperature for 30 minutes, the dimethylformamide was removed at 60° C. under vacuum. Then, 1 liter of water was added to the residue and the mixture was extracted with two 1.5 liter portions of ethyl acetate. The ethyl acetate extract was washed with two 700 ml. portions of water, dried over magnesium sulfate and evaporated under vacuum. After recrystallization of the residue from alcohol, there was obtained N-ethyl-2,6-dimethoxy-4-(methoxycarbonyl)-carbanilic acid benzyl ester having a melting point of 85°-86° C.
WORKUP
后处理
- additionA suspension of 103 g
- additionsubsequently treated with 56.2 g
- temperatureice-cooling
- customthe dimethylformamide was removed at 60° C. under vacuum
- additionThen, 1 liter of water was added to the residue
- extractionthe mixture was extracted with two 1.5 liter portions of ethyl acetate
- extractionThe ethyl acetate extract
- washwas washed with two 700 ml
- dry with materialportions of water, dried over magnesium sulfate
- customevaporated under vacuum
- customAfter recrystallization of the residue from alcohol