HRID1731885

反应详情

EQUATION

反应方程式

HRID 1731885 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 230 mg (5 mmole) of 1-(4-oxo-4-[4-fluorophenyl]butyl)-3-(3-hydroxyphenyl)piperidine and 193 mg (5 mmole) of sodium borohydride in 20 ml of methanol was stirred at room temperature overnight. The solvent was removed by evaporation in vacuo, and the residue was partitioned between ethyl acetate and water. The layers were separated, the aqueous phase was further extracted with ethyl acetate, and all the ethyl acetate phases were combined. The resulting ethyl acetate solution was washed with water, followed by saturated sodium chloride, and then it was dried (MgSO4) and evaporated in vacuo. The residue was chromatographed on 150 ml of silica gel, eluting with chloroform/methanol (9:1). The product-containing fractions were combined and evaporated in vacuo to give 125 mg (67% yield) of the title compound as a foam, containing chloroform of solvation.

WORKUP

后处理

  1. customThe solvent was removed by evaporation in vacuo
  2. customthe residue was partitioned between ethyl acetate and water
  3. customThe layers were separated
  4. extractionthe aqueous phase was further extracted with ethyl acetate
  5. washThe resulting ethyl acetate solution was washed with water
  6. dry with materialit was dried (MgSO4)
  7. customevaporated in vacuo
  8. customThe residue was chromatographed on 150 ml of silica gel
  9. washeluting with chloroform/methanol (9:1)
  10. customevaporated in vacuo