HRID2212997

反应详情

EQUATION

反应方程式

HRID 2212997 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Benzyl bromide (52.4 mL, 441 mmol) was added to a solution of 4-(4-fluorophenyl)pyridine (Description 9, 50.87 g, 294 mmol) in acetone (500 mL) and mixture was heated under reflux for 3 days. The mixture was cooled to room temperature and the solid was collected, washed with acetone and diethyl ether and dried in vacuo. The solid was dissolved in methanol (400 mL) and water (100 mL), cooled to 0° C. and sodium borohydride (20.6 g, 542 mmol) was added in portions. The mixture was stirred at room temperature for 1 hour, then heated under reflux for 18 hours. The mixture was cooled and the solvent was evaporated under reduced pressure. Dichloromethane (300 mL) and water (200 mL) were added and the layers were separated. The organic layer was dried (MgSO4) and the solvent was evaporated under reduced pressure to give the title compound as a light brown oil (61.5 g, 78%). m/z (ES+) 268 (M+1).

WORKUP

后处理

  1. temperaturewas heated
  2. temperatureunder reflux for 3 days
  3. customthe solid was collected
  4. washwashed with acetone and diethyl ether
  5. customdried in vacuo
  6. dissolutionThe solid was dissolved in methanol (400 mL)
  7. temperaturewater (100 mL), cooled to 0° C.
  8. temperatureheated
  9. temperatureunder reflux for 18 hours
  10. temperatureThe mixture was cooled
  11. customthe solvent was evaporated under reduced pressure
  12. additionDichloromethane (300 mL) and water (200 mL) were added
  13. customthe layers were separated
  14. dry with materialThe organic layer was dried (MgSO4)
  15. customthe solvent was evaporated under reduced pressure