HRID2334

反应详情

EQUATION

反应方程式

HRID 2334 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

Methyl(3-amino)benzoate (4.5 g, 29.8 mmol) was taken up in DCM (10 ml) and pyridine (1 ml) at 0° C. 4-Pentenoyl chloride (freshly prepared from 4-pentenoic acid (3.0 g, 29.97 mmol) and thionyl chloride (6.6 ml) at r.t. for 1 h, evaporated and azeotroped with DCM) was added dropwise in DCM (3 ml). The mixture was allowed to warm to r.t. and stirred overnight. The mixture was evaporated and partitioned between EtOAc and 1M HCl. The organic portion was washed with 5% KHCO3 and brine, filtered (Whatman® 1PS, phase separator), and evaporated. The residue was chromatographed (eluant 30% EtOAc in hexanes) to provide a colourless oil (2.20 g, 32%).

WORKUP

后处理

  1. customat 0° C
  2. customevaporated
  3. customazeotroped with DCM)
  4. additionwas added dropwise in DCM (3 ml)
  5. customThe mixture was evaporated
  6. custompartitioned between EtOAc and 1M HCl
  7. washThe organic portion was washed with 5% KHCO3 and brine
  8. filtrationfiltered (Whatman® 1PS, phase separator)
  9. customevaporated
  10. customThe residue was chromatographed (eluant 30% EtOAc in hexanes)