HRID2105280

反应详情

EQUATION

反应方程式

HRID 2105280 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

To a solution of 3-bromonitrobenzene (2.02 g, 10 mmol) in toluene (33 mL) and pyrrolidine (1.0 mL, 12 mmol) was added sodium t-butoxide (1.92 g, 20 mmol) and the solution was deoxygenated by passing a nitrogen through the solution at room temperature for 15 minutes. BINAP and tris(dibenzylideneacetone)dipalladium(0) complex were subsequently added as a solid and the nitrogen bubbling was continued for an additional 5 minutes. The mixture was heated at 100° C. overnight. The reaction mixture was then cooled and partitioned between water and ethyl acetate. The organic layer was washed once with brine solution and dried over anhydrous sodium sulfate. The ethyl acetate was decanted and evaporated under reduced pressure to give the desired 1-(3-nitrophenyl)pyrrolidine as a red oil (1.5 g, 79%).

WORKUP

后处理

  1. customthe solution was deoxygenated
  2. customat room temperature
  3. customfor 15 minutes
  4. additionBINAP and tris(dibenzylideneacetone)dipalladium(0) complex were subsequently added as a solid
  5. temperatureThe reaction mixture was then cooled
  6. custompartitioned between water and ethyl acetate
  7. washThe organic layer was washed once with brine solution
  8. dry with materialdried over anhydrous sodium sulfate
  9. customThe ethyl acetate was decanted
  10. customevaporated under reduced pressure