HRID1478546
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
To a stirred mixture of 2,6-dibromopyridin-3-ol (47.3 g, 0.188 mol) and but-3-en-1-ol (13.8 g, 0.191 mol) in anhydrous THF (200 ml) at 0° C. was added PPh3 (59.4 g, 0.226 mol), followed by diethyl azodicarboxylate (41.77 g, 0.207 mol). The mixture was heated at reflux for 1 h and then concentrated in vacuo to give a dark brown oil. The oil was dissolved in EtOAc, washed with saturated NaHCO3 solution and brine, dried with Na2SO4, and concentrated in vacuo. Petroleum (300 ml) was added to the crude product mixture. The white solid was removed by filtration, and the filtrate was purified by silica gel chromatography (petroleum/EtOAc, 30/1) to afford the title compound as an oil.
WORKUP
后处理
- temperatureThe mixture was heated
- temperatureat reflux for 1 h
- concentrationconcentrated in vacuo
- customto give a dark brown oil
- washwashed with saturated NaHCO3 solution and brine
- dry with materialdried with Na2SO4
- concentrationconcentrated in vacuo
- additionPetroleum (300 ml) was added to the crude product mixture
- customThe white solid was removed by filtration
- customthe filtrate was purified by silica gel chromatography (petroleum/EtOAc, 30/1)