HRID552795

反应详情

EQUATION

反应方程式

HRID 552795 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

A solution of (S)-3-(tert-butoxycarbonyl)-4-(2,2-dimethylbenzo[d][1,3]dioxol-5-yl)-2-oxobutyl acetate (3270 mg, 8311 μmol) in 100 mL of ethanol was cooled to −78° C. and added to a solution of lithium aluminum tri-tert-butoxyhydride (16623 μl, 16623 μmol) in 45 mL of ethanol at −78 C dropwise via a cannula over 10 minutes. After stirring at −78° C. for 2 hours the reaction was quenched with 25 mL of 1 N HCl and diluted with ethyl acetate (500 mL). The mixture was poured into 200 mL of water, the layers were separated and the aqueous layer was extracted with ethyl acetate (3×100 mL). The combined organics were washed with water, brine, and dried over sodium sulfate and concentrated to provide (2S,3S)-3-(tert-butoxycarbonyl)-4-(2,2-dimethylbenzo[d][1,3]dioxol-5-yl)-2-hydroxybutyl acetate (3220 mg, 98% yield) as a white solid.

WORKUP

后处理

  1. customwas quenched with 25 mL of 1 N HCl
  2. additiondiluted with ethyl acetate (500 mL)
  3. additionThe mixture was poured into 200 mL of water
  4. customthe layers were separated
  5. extractionthe aqueous layer was extracted with ethyl acetate (3×100 mL)
  6. washThe combined organics were washed with water, brine
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated