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
1-Ethoxycarbonylmethyl-3-hydroxypyrid-2-one (10 g) is dissolved in methanol/water (9:1 v/v) (400 ml). To this solution is added benzyl chloride (3 molar excess) and NaOH until the pH is above 12. The mixture is then refluxed for six hours to give a clear orange solution. The methanol is removed by rotary evaporation and the aqueous solution is extracted with dichloromethane to remove excess benzyl chloride. The aqueous phase is diluted slightly by adding extra water and then acidified to pH 2 using concentrated hydrochloric acid which results in the precipitation of a beige solid. The mixture is cooled and the precipitate filtered off and washed with diethyl ether. The crude product is recrystallised from ethanol to give 3-benzyloxy-1-carboxymethylpyrid2-one (5.4 g, 41%), m.p. 176°-177° C.
WORKUP
后处理
- temperatureThe mixture is then refluxed for six hours
- customto give a clear orange solution
- customThe methanol is removed by rotary evaporation
- extractionthe aqueous solution is extracted with dichloromethane
- customto remove excess benzyl chloride
- additionThe aqueous phase is diluted slightly
- additionby adding extra water
- customresults in the precipitation of a beige solid
- temperatureThe mixture is cooled
- filtrationthe precipitate filtered off
- washwashed with diethyl ether
- customThe crude product is recrystallised from ethanol