HRID1155836

反应详情

EQUATION

反应方程式

HRID 1155836 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a 0° C. solution of 7.0 mmols. of 3-phenylpropylmagnesium bromide in 7 ml. of tetrahydrofuran is slowly added a solution of 2.48 g. (5.0 mmols) of 1-benzyl-3-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]-4-piperidone in 10 ml. of tetrahydrofuran. The resultant mixture is stirred for one hour and is then added to 250 ml. of saturated ammonium chloride-250 ml. ether. The ether phase is dried over magnesium sulfate and evaporated. The residue is purified via column chromatography on 200 g. of silica gel eluted with 50% ether-cyclohexane to yield the title compound.

WORKUP

后处理

  1. customTo a 0° C.
  2. additionis then added to 250 ml
  3. dry with materialThe ether phase is dried over magnesium sulfate
  4. customevaporated
  5. customThe residue is purified via column chromatography on 200 g
  6. washof silica gel eluted with 50% ether-cyclohexane