HRID1809858

反应详情

EQUATION

反应方程式

HRID 1809858 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

To a solution of 26 g (77 mmol) of benzyl 3-[(tert-butoxycarbonyl)amino]-4-hydroxypyrrolidine-1-carboxylate in 120 mL of THF was added 5 g (211 mmol) of sodium hydride at 0° C. The reaction mixture was stirred at 0° C. for 1 h, then 10 mL (115 mmol) of allyl bromide was added. The reaction mixture was warmed up to room temperature and continuously stirred at room temperature overnight. Water (50 mL) was added to quench the reaction. The organic phase was separated, and the aqueous layer was extracted with ethyl acetate twice (100 mL×2). The combined extracts were washed with brine, dried over Na2SO4, evaporated under reduced pressure. Chromatography on silica gel column with 25% EtOAc-hexane provided the title compound (21.3 g, 73%). MS (M+H)+377.

WORKUP

后处理

  1. temperatureThe reaction mixture was warmed up to room temperature
  2. stirringcontinuously stirred at room temperature overnight
  3. customto quench
  4. customthe reaction
  5. customThe organic phase was separated
  6. extractionthe aqueous layer was extracted with ethyl acetate twice (100 mL×2)
  7. washThe combined extracts were washed with brine
  8. dry with materialdried over Na2SO4
  9. customevaporated under reduced pressure