Reacción #657266
ord-000a72fb152148a0ba487b523f8e51a4
Ecuación de reacción
Condiciones de reacción
Tratamiento posterior
- 1OtroAfter completion of the reaction
- 2Otrothe THF and the toluene were removed
- 3ExtracciónThe reaction solution was extracted with dichloromethane and water
- 4workup.DISTILLATIONdistilled under reduced pressure
- 5OtroThe resulting residue was purified by silica gel column chromatography
- 6workup.DISTILLATIONThe eluate was distilled under reduced pressure
- 7OtroThe residue was recrystallized from dichloromethane and petroleum ether
- 8Filtraciónfiltered
Procedimiento
3-Methylphenyl borate (1.3 mmol), 2-chloro-3,6-dimethylquinoline (1 mmol), tetrakis(triphenylphosphine)palladium(O) (0.05 mmol) and potassium carbonate (3 mmol) were dissolved in THF (30 mL) and H2O (10 mL). The resulting solution was stirred in a bath at 100° C. for 24 hours. After completion of the reaction, the THF and the toluene were removed. The reaction solution was extracted with dichloromethane and water, and distilled under reduced pressure. The resulting residue was purified by silica gel column chromatography. The eluate was distilled under reduced pressure. The residue was recrystallized from dichloromethane and petroleum ether and filtered to yield 2-(3-methylphenyl)-3,6-dimethylquinoline as a solid.