HRID279440

反应详情

EQUATION

反应方程式

HRID 279440 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

Dichloroethane (50 ml), thionyl chloride (6.54 g, 0.055 mol) and dimethylformamide (0.25 ml) were added to 2-phenoxymethylbenzoic acid (11.41 g, 0.05 mol), and the mixture was stirred at 80° C. for 2 hours. After completion of the reaction, the mixture was concentrated under reduced pressure, and the residue was dissolved in dichloromethane (25 ml). The solution was added to a mixture of ethoxyamine hydrochloride (5.85 g, 0.06 mol), pyridine (9.89 g, 0.125 mol) and dry dichloromethane (50 ml) under ice-cooling over 20 minutes, and then the resulting mixture was stirred at room temperature for 2 hours. After completion of the reaction, water (200 ml) was added, adjusted to pH<2 with conc. hydrochloric acid, and extracted with dichloromethane. The dichloromethane layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. Acetonitrile (150 ml), triphenylphosphine (20.98 g, 0.08 mol) and carbon tetrachloride (24.61 g, 0.16 mol) were added to the residue, and the mixture was stirred under reflux for 1.5 hours. After completion of the reaction, the mixture was concentrated under reduced pressure, and the residue was purified by silica gel chromatography (ethyl acetate/n-hexane) to give α-ethoxyimino-2-phenoxymethylbenzyl chloride (13.51 g, 93.2%) as a colorless oil.

WORKUP

后处理

  1. customAfter completion of the reaction
  2. concentrationthe mixture was concentrated under reduced pressure
  3. dissolutionthe residue was dissolved in dichloromethane (25 ml)
  4. temperaturecooling over 20 minutes
  5. stirringthe resulting mixture was stirred at room temperature for 2 hours
  6. additionwas added
  7. extractionextracted with dichloromethane
  8. dry with materialThe dichloromethane layer was dried over anhydrous magnesium sulfate
  9. concentrationconcentrated under reduced pressure
  10. stirringthe mixture was stirred
  11. temperatureunder reflux for 1.5 hours
  12. customAfter completion of the reaction
  13. concentrationthe mixture was concentrated under reduced pressure
  14. customthe residue was purified by silica gel chromatography (ethyl acetate/n-hexane)