HRID1024537

反应详情

EQUATION

反应方程式

HRID 1024537 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A mechanically stirred solution of bromoacetylene 5 (35 g, 121 mmol) and ethynylfuran 8 (23% w/w, 16.7 g, 182 mmol) in 400 mL of pyrrolidine under nitrogen was cooled via ice-water bath. Copper (I) iodide (3.69 g, 19 mmol) was added in one portion and after 5 min the cooling bath was removed and the homogeneous mixture was stirred an additional 1 h. The dark red reaction was quenched by addition of 850 mL of water with stirring. The orange-yellow suspension was extracted with 4×300 ml of diethyl ether. The combined organic layers were washed with 3×100 mL of water and 100 mL of brine, dried over sodium sulfate, and concentrated in vacuo to a dark red oil. The residue was resuspended in 100 mL of 10% ethyl acetate in hexanes and passed through a pad of silica gel in a flitted funnel. The pad was washed with an additional 4×50 mL of solvent and concentrated in vacuo to give 21.0 g of crude 9 as a dark red oil.

WORKUP

后处理

  1. customwas removed
  2. customThe dark red reaction
  3. customwas quenched by addition of 850 mL of water
  4. stirringwith stirring
  5. extractionThe orange-yellow suspension was extracted with 4×300 ml of diethyl ether
  6. washThe combined organic layers were washed with 3×100 mL of water and 100 mL of brine
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated in vacuo to a dark red oil
  9. custompassed through a pad of silica gel in a flitted funnel
  10. washThe pad was washed with an additional 4×50 mL of solvent
  11. concentrationconcentrated in vacuo