HRID1582943

反应详情

EQUATION

反应方程式

HRID 1582943 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

To a stirred solution of p-acetylbenzonitrile (3.0 g, 20.0 mmol) in tetrahydrofuran at −78° C. was added drop-wise a solution of 3.0 M methyl magnesium chloride in tetrahydrofuran (7.6, 23.0 mmol). The reaction mixture was stirred at −78° C. for 3 hours and then quenched with methanol added drop-wise. The reaction mixture was thereafter poured into water (200 ml), acidified with oxalic acid added portion-wise, and then extracted with diethyl ether (2×200 ml). The organic extracts were combined, washed with water (1×40 ml), brine (1×40 ml), dried over magnesium sulfate (MgSO4), and then concentrated to give an oil. The oil product was purified using chromatography on silica gel, eluting with ethyl acetate/hexane (1:5), to give 1.4 g of 4-(1-Hydroxy-1-methyl-ethyl)-benzonitrile as a clear oil.

WORKUP

后处理

  1. customquenched with methanol added drop-wise
  2. additionThe reaction mixture was thereafter poured into water (200 ml)
  3. extractionextracted with diethyl ether (2×200 ml)
  4. washwashed with water (1×40 ml), brine (1×40 ml)
  5. dry with materialdried over magnesium sulfate (MgSO4)
  6. concentrationconcentrated
  7. customto give an oil
  8. customThe oil product was purified
  9. washeluting with ethyl acetate/hexane (1:5)