HRID495108

反应详情

EQUATION

反应方程式

HRID 495108 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

3-(4-Methoxyphenoxy)propylamine (34 mg) was dissolved in methanol (3 mL), and a solution (2 mL) of n-butyl (R)-2-(3-formylphenoxy)butyrate (50 mg) in methanol was added thereto under stirring at room temperature. The mixture was further stirred at 80° C. for 12 hours. Subsequently, an aqueous solution (0.5 mL) of sodium borohydride (7 mg) was added to the solution at room temperature, and the mixture was stirred for 30 minutes. The reaction solution was concentrated under reduced pressure, and chloroform was added to the concentrated product. The formed organic layer was washed with water. The washed organic layer was dried over sodium sulfate anhydrate, and concentrated under reduced pressure, to thereby yield 81 mg of a pale yellow, oily substance. The entirety of the substance was employed in the following reaction without any further treatment.

WORKUP

后处理

  1. stirringThe mixture was further stirred at 80° C. for 12 hours
  2. stirringthe mixture was stirred for 30 minutes
  3. concentrationThe reaction solution was concentrated under reduced pressure, and chloroform
  4. additionwas added to the concentrated product
  5. washThe formed organic layer was washed with water
  6. dry with materialThe washed organic layer was dried over sodium sulfate anhydrate
  7. concentrationconcentrated under reduced pressure
  8. customThe entirety of the substance was employed in the following reaction without any further treatment