HRID1599436
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 solution of 1-diphenylmethyl-3-methanesulphonyloxyazetidine (Preparation 1(b)) (24.46 g, 7.72 mmol), potassium carbonate (32 g, 3 mol equiv) and morpholine (7.34 ml, 1.09 mol equiv) in acetonitrile (200 ml) was heated under reflux for 4 hours. The solution was then cooled to room temperature, water (50 ml) added and the mixture concentrated in vacuo. The residue was then partitioned between ethyl acetate (400 ml) and water (400 ml) and the organic phase washed with water (2×400 ml). The organic phase was dried over MgSO4, and the solvent removed in vacuo. The residue was chromatographed using silica gel eluting with hexane: diethyl ether (1:1) to give the title compound (16.5 g).
WORKUP
后处理
- temperatureunder reflux for 4 hours
- concentrationthe mixture concentrated in vacuo
- customThe residue was then partitioned between ethyl acetate (400 ml) and water (400 ml)
- washthe organic phase washed with water (2×400 ml)
- dry with materialThe organic phase was dried over MgSO4
- customthe solvent removed in vacuo
- customThe residue was chromatographed