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
6-Iodo-3,4-dihydroquinolin-2(1H)-one (1.50 g; 5.50 mmol), sodium cyanide (0.54 g; 11.0 mmol), copper (I) iodide (0.105 g; 0.5 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.32 g; 0.3 mmol) were combined in a flask equipped with a reflux condenser. The flask was subjected to several evacuation-nitrogen purge cycles followed by the addition of acetonitrile (25 mL). The reaction was heated to reflux for 5 hours. After cooling, the reaction was diluted with ethyl acetate (200 mL), filtered through CELITE diatomaceous earth and rinsed with copious amounts of ethyl acetate. The organic solution was washed twice with brine (50 mL), dried over sodium sulfate, filtered through a fritted funnel, and the volatiles were removed under vacuum. The crude residue was crystallized from methanol, which afforded the title compound.
WORKUP
后处理
- customequipped with a reflux condenser
- custompurge cycles
- additionfollowed by the addition of acetonitrile (25 mL)
- temperatureThe reaction was heated
- temperatureto reflux for 5 hours
- temperatureAfter cooling
- additionthe reaction was diluted with ethyl acetate (200 mL)
- filtrationfiltered through CELITE diatomaceous earth
- washrinsed with copious amounts of ethyl acetate
- washThe organic solution was washed twice with brine (50 mL)
- dry with materialdried over sodium sulfate
- filtrationfiltered through a fritted funnel
- customthe volatiles were removed under vacuum
- customThe crude residue was crystallized from methanol, which