HRID983765

反应详情

EQUATION

反应方程式

HRID 983765 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

To 0.90 ml (3.0 mmol) of tetraisopropoxytitanium and 5 ml of n-butyl ether solution containing allyl bromide (3.0 mmol) was added dropwise at −78° C. 6.2 ml of 0.97M n-butyl ether solution containing isopropylmagnesium bromide (6.0 mmol). After stirring at −50° C. to −40° C. for 1 hour, the reaction liquid was given 0.21 ml (2.1 mmol) of benzaldehyde and heated to 0° C. over 30 minutes. With 10 ml of 3N hydrochloric acid added, the solution was heated to room temperature and separated into layers. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate. After drying with anhydrous magnesium sulfate, the solution was freed of solvent by vacuum distillation. The residues were purified by silica gel chromatography. Thus there was obtained 252 mg of 1-phenyl-3-buten-1-ol (81% yields based on benzaldehyde).

WORKUP

后处理

  1. additionwas added dropwise at −78° C
  2. customthe reaction liquid
  3. temperaturethe solution was heated to room temperature
  4. customseparated into layers
  5. washThe organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate
  6. dry with materialAfter drying with anhydrous magnesium sulfate
  7. distillationthe solution was freed of solvent by vacuum distillation
  8. customThe residues were purified by silica gel chromatography