HRID1415761

反应详情

EQUATION

反应方程式

HRID 1415761 的结构方程式

PROCEDURE

实验过程

4.42 g (15.8 mmol) of methyl 2-(4-methylthiophenacyl)acetoacetate [prepared as described in step (i) above] were dissolved in 150 ml of methylene chloride, and 7.77 g (31.5 mmol) of 70% m-chloroperbenzoic acid were added to the resulting solution, whilst ice-cooling. The mixture was then stirred at room temperature for 1 hour. 30 ml of a 10% w/v aqueous solution of sodium thiosulfate were added to the mixture, and the mixture was vigorously shaken, after which it separated into liquid phases. The organic layer was separated and washed with a saturated aqueous solution of sodium hydrogencarbonate and with a saturated aqueous solution of sodium chloride, in that order, after which it was dried over anhydrous magnesium sulfate and the solvent was then removed by distillation under reduced pressure. The residue was applied to a silica gel chromatography column and eluted with a 1:1 by volume mixture of ethyl acetate and hexane, to give 3.65 g (yield 74%) of the title compound as a slightly yellow powder.

WORKUP

后处理

  1. temperaturecooling
  2. stirringthe mixture was vigorously shaken
  3. customafter which it separated into liquid phases
  4. customThe organic layer was separated
  5. washwashed with a saturated aqueous solution of sodium hydrogencarbonate and with a saturated aqueous solution of sodium chloride, in that order
  6. dry with materialafter which it was dried over anhydrous magnesium sulfate
  7. customthe solvent was then removed by distillation under reduced pressure
  8. washeluted with a 1:1 by volume mixture of ethyl acetate and hexane