HRID1650069

反应详情

EQUATION

反应方程式

HRID 1650069 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

A solution of 3.89 g. (10 mmoles) of 2-(3-benzyloxy-4-bromophenyl)-2-methyloctane in 10 ml. of tetrahydrofuran was slowly added to 360 mg. (14.4 mmoles) of 70-80 mesh magnesium metal. The resulting mixture was refluxed for 30 minutes and then cooled to 0° C. To this solution was slowly added a solution of 1.40 g. (10 mmoles) of 3-ethoxy-2-cyclohexen-1-one in 3 ml. of tetrahydrofuran. The reaction mixture was stirred for 30 minutes at 0° C. and then quenched by the addition of 20 ml. of 1N sulfuric acid and heating on the steam bath for 30 minutes. It was then cooled and added to 200 ml. of ether-200 ml. of water. The organic extract was washed successively with 200 ml. of saturated sodium bicarbonate and 200 ml. of saturated sodium chloride, dried over magnesium sulfate and evaporated to an oil. The crude product was purified via column chromatography on 170 g. of silica gel eluted with 1:1 ether:pentane to yield 2.5 g. (54%) of the title compound as an oil.

WORKUP

后处理

  1. temperatureThe resulting mixture was refluxed for 30 minutes
  2. additionTo this solution was slowly added a solution of 1.40 g
  3. customquenched by the addition of 20 ml
  4. temperatureof 1N sulfuric acid and heating on the steam bath for 30 minutes
  5. temperatureIt was then cooled
  6. additionadded to 200 ml
  7. extractionThe organic extract
  8. washwas washed successively with 200 ml
  9. dry with materialof saturated sodium chloride, dried over magnesium sulfate
  10. customevaporated to an oil
  11. customThe crude product was purified via column chromatography on 170 g
  12. washof silica gel eluted with 1:1 ether
  13. custompentane to yield 2.5 g