HRID2334
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
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
- customat 0° C
- customevaporated
- customazeotroped with DCM)
- additionwas added dropwise in DCM (3 ml)
- customThe mixture was evaporated
- custompartitioned between EtOAc and 1M HCl
- washThe organic portion was washed with 5% KHCO3 and brine
- filtrationfiltered (Whatman® 1PS, phase separator)
- customevaporated
- customThe residue was chromatographed (eluant 30% EtOAc in hexanes)