HRID983764

反应详情

EQUATION

反应方程式

HRID 983764 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To 0.30 ml (1.0 mmol) of tetraisopropoxytitanium and 5 ml of ethyl ether solution containing allyl bromide (1.0 mmol) was added dropwise at −50° C. 1.67 ml of 1.2M ethyl ether solution containing isopropylmagnesium bromide (2.0 mmol). Upon stirring at −50° C. to −40° C. for 1 hour, the reaction liquid turned from yellow into brown. To the reaction liquid was added 0.071 ml (0.7 mmol) of benzaldehyde at −45° C. to −40° C. The temperature was raised to −10° C. to 0° C. over 30 minutes. With 5 ml of 1N 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 97 mg of 1-phenyl-3-buten-1-ol (94% yields based on benzaldehyde).

WORKUP

后处理

  1. additionwas added dropwise at −50° C
  2. customthe reaction liquid
  3. customTo the reaction liquid
  4. temperatureThe temperature was raised to −10° C. to 0° C. over 30 minutes
  5. customseparated into layers
  6. washThe organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate
  7. dry with materialAfter drying with anhydrous magnesium sulfate
  8. distillationthe solution was freed of solvent by vacuum distillation
  9. customThe residues were purified by silica gel chromatography