HRID1972191

反应详情

EQUATION

反应方程式

HRID 1972191 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

In a 100 mL round bottom flask is added methyltriphenylphosphonium bromide (2.79 g, 7.8 mmol) and anhydrous ethyl ether (40 mL). The suspension is then cooled down to −78° C. and BuLi (6.77 mmol, 4.23 mL 1.6 M solution in hexane) is added dropwise. After the addition, the bright yellow mixture is warmed up to 0° C. and stirred for 30 min and cooled down to −78° C. again. To this mixture, a solution of 3-fluoro-5-trifluoromethyl-benzaldehyde (1 g, 5.2 mmol) in anhydrous ethyl ether (6 mL) is added drop by drop. After the addition, the mixture is slowly warmed up to room temperature and stirred for 14 hr. The precipitate is removed by filtration and washed with ethyl ether (2×5 mL). The filtrate is concentrated by distilling off ethyl ether at ˜60° C. bath temperature. The resulted higher boiling point liquid is purified by pass through a short column (silica gel) with hexane. After removing the hexane under vacuum (˜150 mmHg), the resulted crude 1-fluoro-3-trifluoromethyl-5-vinyl-benzene is used directly for next step.

WORKUP

后处理

  1. additionAfter the addition
  2. temperaturethe bright yellow mixture is warmed up to 0° C.
  3. temperaturecooled down to −78° C. again
  4. additionAfter the addition
  5. temperaturethe mixture is slowly warmed up to room temperature
  6. stirringstirred for 14 hr
  7. customThe precipitate is removed by filtration
  8. washwashed with ethyl ether (2×5 mL)
  9. concentrationThe filtrate is concentrated
  10. distillationby distilling off ethyl ether at ˜60° C. bath temperature
  11. customThe resulted higher boiling point liquid
  12. customis purified by pass through a short column (silica gel) with hexane
  13. customAfter removing the hexane under vacuum (˜150 mmHg)