反应 #554331
ord-784059b961f242cf92fa0aec34b6e2e1
反应方程式
反应条件
后处理
- 1温度under cooling
- 2workup.ADDITIONAfter the dropwise addition the mixture
- 3温度under cooling
- 4workup.WAITfor one hour at room temperature
- 5其他the organic layer was separated
- 6洗涤washed successively with a saturated aqueous solution of sodium hydrogen carbonate (15 ml), water (15 ml)
- 7干燥a saturated aqueous solution of edible salt (15 ml), dried over sodium sulfate
- 8过滤filtered
- 9浓缩The filtrate is concentrated to dryness under reduced pressure
- 10其他The residue is purified by column chromatography on silica gel (n-hexane-dichloromethanemethanol, 6:4:1)
实验过程
tert-Butoxycarbonyl-L-prolinal dimethyl acetal (1.0 g, 4.08 mmol) is stirred for one hour at room temperature in 10% HCl-methanol (8.2 ml) and the mixture is evaporated to dryness under reduced pressure to give quantitatively L-prolinal dimethylacetal hydrochloride as a solid. The product is dissolved in dimethylformamide (5 ml) containing p-anisic acid (938 mg, 6.16 mmol) and diethyl-phosphoryl cyanide (0.65 ml, 8.25 mmol). To the solution is added dropwise triethylamine (1.15 ml, 8.25 mmol) under cooling and agitation in an ice-methanol bath. After the dropwise addition the mixture is stirred for one hour under cooling and then for one hour at room temperature. Benzene-ethyl acetate (2:1, 150 ml) is added to the reaction mixture and the organic layer was separated, washed successively with a saturated aqueous solution of sodium hydrogen carbonate (15 ml), water (15 ml) and a saturated aqueous solution of edible salt (15 ml), dried over sodium sulfate and filtered. The filtrate is concentrated to dryness under reduced pressure. The residue is purified by column chromatography on silica gel (n-hexane-dichloromethanemethanol, 6:4:1) to give 747 mg (65%) of the title compound as white crystals.