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
CONDITIONS
反应条件
- 温度
- -70 °C
PROCEDURE
实验过程
The above-obtained solution was cooled to -70° C. in a dry ice-acetone bath. To this solution were successively added 88 mg (1 mmole) of methyl glyoxylate and 0.168 g (2 mmole) of 1-methoxy-1,3-butadiene. Reaction was then allowed to proceed at -30° C. for 3 hours, and 10 ml of a sodium hydrogencarbonate aqueous solution was added to the reaction mixture to terminate the reaction. This reaction mixture was filtered through Celite and then subjected to extraction once with a 20 ml of diethyl ether and twice with 20 ml of ethyl acetate. The extract was dried over anhydrous magnesium sulfate. Thereafter, the solvent was removed by evaporation, and the residue was purified by silica gel column chromatography (200 mesh; developing solvent: hexane/ethyl acetate=10/1), thereby obtaining 0.12 g of desired optically active 2-methoxy-6-methoxycarbonyl-5,6-dihydropyran (yield: 79%).
WORKUP
后处理
- customReaction
- customto terminate
- customthe reaction
- filtrationThis reaction mixture was filtered through Celite
- extractionsubjected to extraction once with a 20 ml of diethyl ether and twice with 20 ml of ethyl acetate
- dry with materialThe extract was dried over anhydrous magnesium sulfate
- customThereafter, the solvent was removed by evaporation
- customthe residue was purified by silica gel column chromatography (200 mesh; developing solvent: hexane/ethyl acetate=10/1)
- customobtaining 0.12 g