HRID324456

反应详情

EQUATION

反应方程式

HRID 324456 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

n-Butyllithium (34 ml of a 2.5M solution in hexanes) was added to a solution of 1-bromo-3-ethylbenzene (15 g) in tetrahydrofuran (320 ml) at −78° C. After 1 hour N,N-dimethylformamide (15 ml) was added. The mixture was stirred at −78° C. for 1 hour and allowed to warm to room temperature. The mixture was quenched with aqueous ammonium chloride and partitioned between ethyl acetate and water. The organic phase was dried (MgSO4) and evaporated. The residue was dissolved in methanol (250 ml) and treated with sodium borohydride (1.51 g) portionwise. The mixture was stirred at room temperature for 16 hours, quenched with 2M HCl (100 ml) and stirred for 4 hours. The mixture was concentrated under reduced pressure and the residue partitioned between ethyl acetate and 2M HCl. The organic phase was dried (MgSO4), evaporated and the residue purified by chromatography eluting with 5-10% ethyl acetate in isohexane.

WORKUP

后处理

  1. temperatureto warm to room temperature
  2. customThe mixture was quenched with aqueous ammonium chloride
  3. custompartitioned between ethyl acetate and water
  4. dry with materialThe organic phase was dried (MgSO4)
  5. customevaporated
  6. dissolutionThe residue was dissolved in methanol (250 ml)
  7. additiontreated with sodium borohydride (1.51 g) portionwise
  8. stirringThe mixture was stirred at room temperature for 16 hours
  9. customquenched with 2M HCl (100 ml)
  10. stirringstirred for 4 hours
  11. concentrationThe mixture was concentrated under reduced pressure
  12. customthe residue partitioned between ethyl acetate and 2M HCl
  13. dry with materialThe organic phase was dried (MgSO4)
  14. customevaporated
  15. customthe residue purified by chromatography
  16. washeluting with 5-10% ethyl acetate in isohexane