HRID712397

反应详情

EQUATION

反应方程式

HRID 712397 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
55 °C

PROCEDURE

实验过程

A mixture of NaOH aqueous solution (35 w/w %, 21 mL, aq.), ClCH2CH2Cl (21 mL), benzyl 3,4-dihydroxypyrrolidine-1-carboxylate (1.16 g, 4.9 mmol, 1.0 eq) and TBAB (0.31 g, 0.98 mmol, 0.2 eq) was heated at 55° C. for 48 h in a round-bottom flask. The reaction mixture was cooled to room temperature and poured into water (50 mL), extracted with EtOAc (50 mL). The organic phase was separated from the mixture, and the water phase was extracted with EtOAc (20 mL×3). The combined organic phases were dried over anhydrous Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was purified with a silica gel column chromatography (1:1 (v/v) PE/EtOAc) to give the product as colorless oil (0.50 g, 39%).

WORKUP

后处理

  1. temperatureThe reaction mixture was cooled to room temperature
  2. extractionextracted with EtOAc (50 mL)
  3. customThe organic phase was separated from the mixture
  4. extractionthe water phase was extracted with EtOAc (20 mL×3)
  5. dry with materialThe combined organic phases were dried over anhydrous Na2SO4
  6. filtrationfiltered
  7. concentrationThe filtrate was concentrated in vacuo
  8. customthe residue was purified with a silica gel column chromatography (1:1 (v/v) PE/EtOAc)