HRID18181

反应详情

EQUATION

反应方程式

HRID 18181 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

1-Bromo-3-iodo-5-methyl-2-(3-phenylallyloxy)-benzene (10.86 g, 25 mmol), tetrabutylammonium chloride (7.65 gm, 27.5 mmol), sodium carbonate (6.62 g, 62.46 mmol), sodium formate (1.7 g, 25 mmol), and bis(acetonitrile)dichloropalladium(II) (0.467 g, 1.8 mmol) was added to 50 ml DMF. The mixture was degassed and heated under nitrogen at 80° C. for 105 minutes, then cooled to room temperature. Water was added and the mixture was extracted with a hexanes/ethyl acetate (1:1) mixture. The solution was dried onto 20 gm silica gel, the silica gel was layered over 100 gm silica gel in a fritted funnel and eluted with four 400 ml portions of hexanes. The hexanes was removed under reduced pressure to give 3-benzyl-7-bromo-5-methyl-benzofuran (3.97 g, 52% yield). MS: (M+H)+ 302.

WORKUP

后处理

  1. customThe mixture was degassed
  2. temperaturecooled to room temperature
  3. additionWater was added
  4. extractionthe mixture was extracted with a hexanes/ethyl acetate (1:1) mixture
  5. customThe solution was dried onto 20 gm silica gel
  6. customthe silica gel was layered over 100 gm silica gel in a fritted funnel
  7. washeluted with four 400 ml portions of hexanes
  8. customThe hexanes was removed under reduced pressure