HRID6813

反应详情

EQUATION

反应方程式

HRID 6813 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

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

  1. customequipped with a reflux condenser
  2. custompurge cycles
  3. additionfollowed by the addition of acetonitrile (25 mL)
  4. temperatureThe reaction was heated
  5. temperatureto reflux for 5 hours
  6. temperatureAfter cooling
  7. additionthe reaction was diluted with ethyl acetate (200 mL)
  8. filtrationfiltered through CELITE diatomaceous earth
  9. washrinsed with copious amounts of ethyl acetate
  10. washThe organic solution was washed twice with brine (50 mL)
  11. dry with materialdried over sodium sulfate
  12. filtrationfiltered through a fritted funnel
  13. customthe volatiles were removed under vacuum
  14. customThe crude residue was crystallized from methanol, which