HRID256414

反应详情

EQUATION

反应方程式

HRID 256414 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

Under anhydrous conditions and a nitrogen atmoshere a solution of 8.7 g (0.086 mole) diisopropylamine in 250 ml tetrahydrofuran was cooled to -78° C. and 1.6M n-butyllithium (53.75 ml, 0.086 mole) was added dropwise over ten minutes. The mixture was stirred for 45 minutes, allowed to warm to 0° C. and 12.2 g (0.086 mole) methyl cyclohexancarboxylate was added. Stirring was continued for 45 minutes and then 20 g (0.086 mole) 2-benzyloxybenzyl chloride in 20 ml tetrahydrofuran was added dropwise. The resulting mixture was stirred at room temperature for 24 hours, quenched by addition of 150 ml 3M acetic acid and stirred at room temperature for one week. The mixture was diluted with ethyl ether, washed with sodium bicarbonate solution, brine, dried (MgSO4) and concentrated to a yellow oil, 29.3 g. This was distilled to obtain 20.23 g (70%) of viscous oil, b.p. 135°-140° C. (0.4 Torr).

WORKUP

后处理

  1. temperatureto warm to 0° C.
  2. stirringStirring
  3. waitwas continued for 45 minutes
  4. stirringThe resulting mixture was stirred at room temperature for 24 hours
  5. customquenched by addition of 150 ml 3M acetic acid
  6. stirringstirred at room temperature for one week
  7. additionThe mixture was diluted with ethyl ether
  8. washwashed with sodium bicarbonate solution, brine
  9. dry with materialdried (MgSO4)
  10. concentrationconcentrated to a yellow oil, 29.3 g
  11. distillationThis was distilled