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
To a solution of 0.39 g of the amorphous compound obtained in Example 190, 0.145 g of 1-piperidinethanol and 0.369 g of triphenylphosphine in 5 ml of tetrahydrofuran, was added dropwise a solution of 0.245 g of diethyl azodicarboxylate in 2 ml of tetrahydrofuran with stirring under ice cooling. The mixture was stirred for 2 hours and evaporated to remove the solvent under a reduced pressure, and resulting residue dissolved in 30 ml of ethyl acetate and extracted three times with 10 ml of 1N hydrochloric acid. The aqueous layer was alkallized with sodium bicarbonate and extracted three times with 10 ml of ehtyl acetate, and the organic extract was dried over magnesium sulfate and evaporated to remove the solvent at a reduced pressure. The resulting residue was applied to a silica gel column and eluted with 2% methanol in chloroform, to obtain 0.37 g of the title compound as a colorless oil.
WORKUP
后处理
- stirringThe mixture was stirred for 2 hours
- customevaporated
- customto remove the solvent under a reduced pressure
- customresulting residue
- extractionextracted three times with 10 ml of 1N hydrochloric acid
- extractionextracted three times with 10 ml of ehtyl acetate
- extractionthe organic extract
- dry with materialwas dried over magnesium sulfate
- customevaporated
- customto remove the solvent at a reduced pressure
- washeluted with 2% methanol in chloroform