HRID250195

反应详情

EQUATION

反应方程式

HRID 250195 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
110 °C

PROCEDURE

实验过程

5-methoxybenzofuran (0.48 g) and trifluoro-acetic acid 3-[methyl-(2,2,2-trifluoro-acetyl)-amino]-1-phenyl-propyl ester (0.48 g) were mixed and heated in a sealed tube at 110° C. for 90 minutes. Upon cooling, the reaction mixture was taken up in methanol and treated with excess 1N sodium hydroxide solution, sufficient to form a strongly basic solution. After stirring for 20 minutes, the reaction mixture was concentrated at reduced pressure to remove the bulk of the methanol. The resulting mixture was partitioned between ethyl acetate and water. The layers were separated and the organic layer was evaporated to dryness. Purification by column chromatography (silica gel, dichloromethane (130):methanol (10):ammonium hydroxide (1)) followed by preparative tlc afforded [3-(5-Methoxy-benzofuran-2-yl)-3-phenyl-propyl]-methyl-amine (M+H=296) as the major component.

WORKUP

后处理

  1. temperatureUpon cooling
  2. customsufficient to form a strongly basic solution
  3. concentrationthe reaction mixture was concentrated at reduced pressure
  4. customto remove the bulk of the methanol
  5. customThe resulting mixture was partitioned between ethyl acetate and water
  6. customThe layers were separated
  7. customthe organic layer was evaporated to dryness
  8. customPurification by column chromatography (silica gel, dichloromethane (130):methanol (10):ammonium hydroxide (1))