HRID26061

反应详情

EQUATION

反应方程式

HRID 26061 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
-10 °C

PROCEDURE

实验过程

A solution of 20.0 g. (51.4 mmols) of 1-bromo-2-benzyloxy-4-(1,1-dimethylheptyl)benzene in 75 ml. of tetrahydrofuran is slowly added to 2.5 g. (103 mmols) of 70-80 mesh magnesium metal. The resulting mixture is refluxed for 20 minutes and is then cooled to -10° C. A solution of 9.71 g. (51.4 mmols) of N-benzyl-3-piperidone in 25 ml. of tetrahydrofuran is then added at such a rate that the reaction temperature is maintained below 0° C. The reaction mixture is stirred for 30 minutes following completion of addition and is then added to 500 ml. of saturated ammonium chloride and 500 ml. of ether. The ether extract is washed with two 250 ml. portions of sodium chloride, dried over magnesium sulfate and evaporated to an oil. The oil is purified via column chromatography on 700 g. of silica gel eluted with 50% ether-cyclohexane to yield 17.1 g. (67%) of the title compound as an oil:

WORKUP

后处理

  1. temperatureThe resulting mixture is refluxed for 20 minutes
  2. temperatureis maintained below 0° C
  3. additioncompletion of addition
  4. additionis then added to 500 ml
  5. extractionThe ether extract
  6. washis washed with two 250 ml
  7. dry with materialportions of sodium chloride, dried over magnesium sulfate
  8. customevaporated to an oil
  9. customThe oil is purified via column chromatography on 700 g
  10. washof silica gel eluted with 50% ether-cyclohexane
  11. customto yield 17.1 g