反应 #554331

ord-784059b961f242cf92fa0aec34b6e2e1

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度under cooling
  2. 2
    workup.ADDITIONAfter the dropwise addition the mixture
  3. 3
    温度under cooling
  4. 4
    workup.WAITfor one hour at room temperature
  5. 5
    其他the organic layer was separated
  6. 6
    洗涤washed successively with a saturated aqueous solution of sodium hydrogen carbonate (15 ml), water (15 ml)
  7. 7
    干燥a saturated aqueous solution of edible salt (15 ml), dried over sodium sulfate
  8. 8
    过滤filtered
  9. 9
    浓缩The filtrate is concentrated to dryness under reduced pressure
  10. 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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05158970uspto-grants-1992_10