反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
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
- customwas removed
- customThe dark red reaction
- customwas quenched by addition of 850 mL of water
- stirringwith stirring
- extractionThe orange-yellow suspension was extracted with 4×300 ml of diethyl ether
- washThe combined organic layers were washed with 3×100 mL of water and 100 mL of brine
- dry with materialdried over sodium sulfate
- concentrationconcentrated in vacuo to a dark red oil
- custompassed through a pad of silica gel in a flitted funnel
- washThe pad was washed with an additional 4×50 mL of solvent
- concentrationconcentrated in vacuo