HRID128912

反应详情

EQUATION

反应方程式

HRID 128912 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

Triphenylphosphine (1.05 g), 1-phenylpropyl alcohol (0.54 g) and THF (20 ml) were added to 2-hydroxy-α-(1-imidazolyl)benzaldehyde O-methyloxime (0.43 g), and diethyl azodicarboxylate (0.70 g) was added under ice-cooling over 10 minutes. Then the mixture was stirred at room temperature for 2 hours. After completion of the reaction, ether (100 ml) was added, the mixture was washed with water (80 ml) twice, and the ether layer was concentrated under reduced pressure. The resulting crude product was purified by silica gel chromatography to give α-(1-imidazolyl)-2-(1-phenylpropyloxy)benzaldehyde O-methyloxime (0.63 g) as a colorless oil.

WORKUP

后处理

  1. additionwas added under ice-
  2. temperaturecooling over 10 minutes
  3. additionwas added
  4. washthe mixture was washed with water (80 ml) twice
  5. concentrationthe ether layer was concentrated under reduced pressure
  6. customThe resulting crude product was purified by silica gel chromatography