HRID411142

反应详情

EQUATION

反应方程式

HRID 411142 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A cooled (0° C.) mixture of 4-(1-hydroxy-3-butenyl)benzonitrile (14.6 g, 84.3 mmol) and 3,4-dimethoxyphenol (19.5 g, 125.4 mmol) in toluene (500 mL) was treated with tributylphosphine (32.14 mL of 97% purity, 25.6 g, 126.4 mmol), followed by 1,1′-(azodicarbonyl)dipiperidine (31.8 g, 126.4 mmol). After addition was complete, the reaction mixture thickened and the temperature rose to 15° C. Additional toluene was added (500 mL), and the mixture stirred at rt overnight. The precipitate of tributylphosphine oxide was then removed by filtration and the filtrate concentrated in vacuo to give 65.8 g of crude product. This was purified by chromatography on silica gel, eluting with toluene:methanol (98:2), to yield 17.9 g of the sub-title compound.

WORKUP

后处理

  1. temperatureA cooled
  2. additionAfter addition
  3. customrose to 15° C
  4. customThe precipitate of tributylphosphine oxide was then removed by filtration
  5. concentrationthe filtrate concentrated in vacuo
  6. customto give 65.8 g of crude product
  7. customThis was purified by chromatography on silica gel
  8. washeluting with toluene:methanol (98:2)