HRID132821

反应详情

EQUATION

反应方程式

HRID 132821 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 cold (0° C.) solution of 2,3-dihydro-pyrrole-1-carboxylic acid benzyl ester (example 4, step 5, 300 mg, 1.0 eq.) in diethyl ether was slowly added a solution of diethylzinc in hexanes (1M, 7 mL, 4.75 eq.), followed by chloroiodomethane (1.1 mL, 10 eq.). The reaction mixture was stirred 3 h at 0° C., allowed to warm up to room temperature and stirred an additional 3 h. The reaction mixture was partitioned between an aqueous solution of ammonium chloride and diethyl ether. The aqueous layer was extracted with diethyl ether and the combined organic layers were washed with brine, dried over sodium sulphate and evaporated in vacuo and purified on silica, eluting with a 1:1 to 1:3 gradient of cyclohexane/dichloromethane, to yield 160 mg (50%) of the desired product as colourless oil. MS (m/e): 218.5 (MH+, 100%)

WORKUP

后处理

  1. temperatureto warm up to room temperature
  2. stirringstirred an additional 3 h
  3. customThe reaction mixture was partitioned between an aqueous solution of ammonium chloride and diethyl ether
  4. extractionThe aqueous layer was extracted with diethyl ether
  5. washthe combined organic layers were washed with brine
  6. dry with materialdried over sodium sulphate
  7. customevaporated in vacuo
  8. custompurified on silica
  9. washeluting with a 1:1 to 1:3 gradient of cyclohexane/dichloromethane