HRID3911
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 17.0 parts of 2-amino-4-chloromethyl-6-methoxypyrimidine, 59.5 parts of caesium fluoride and 130 parts of dry dimethylformamide was stirred under reflux for 2 hours. The mixture was cooled and evaporated in vacuo. The residue was taken up in ethyl acetate and the solution was washed four times with water. The organic phase was dried with anhydrous magnesium sulphate, stirred with decolourising charcoal, filtered and evaporated. The crude product was purified by chromatography on silica, eluted with ethyl acetate to give 2-amino-4-fluoromethyl-6-methoxypyrimidine m.p. 119°-121° C.
WORKUP
后处理
- temperatureunder reflux for 2 hours
- temperatureThe mixture was cooled
- customevaporated in vacuo
- washthe solution was washed four times with water
- dry with materialThe organic phase was dried with anhydrous magnesium sulphate
- stirringstirred with decolourising charcoal
- filtrationfiltered
- customevaporated
- customThe crude product was purified by chromatography on silica
- washeluted with ethyl acetate