HRID720835

反应详情

EQUATION

反应方程式

HRID 720835 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A stirred, cooled solution of 1-bromo-3-iodobenzene (31 g) and 3-butyn-ol (7 ml) in acetonitrile (100 ml) and triethylamine (100 ml) was purged with nitrogen for 20 min under nitrogen. Dichlorobis(triphenylphosphine)palladium (500 mg) and cuprous iodide (800 mg) were added. The mixture was stirred for 18 h and then the solvent was removed in-vacuo. The residual oil was triturated with ethyl acetate (200 ml) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on Biotage (90 g) eluting with light petroleum 40–60°-diethyl ether (3:2) to give the title compound (21 g). LCMS RT=3.26 min.

WORKUP

后处理

  1. customwas purged with nitrogen for 20 min under nitrogen
  2. additionDichlorobis(triphenylphosphine)palladium (500 mg) and cuprous iodide (800 mg) were added
  3. customthe solvent was removed in-vacuo
  4. customThe residual oil was triturated with ethyl acetate (200 ml)
  5. filtrationfiltered
  6. customThe filtrate was evaporated to dryness
  7. customthe residue was purified by chromatography on Biotage (90 g)
  8. washeluting with light petroleum 40–60°-diethyl ether (3:2)