반응 #657266

ord-000a72fb152148a0ba487b523f8e51a4

반응 방정식

Cc1cccc(OB([O-])[O-])c1
3-Methylphenyl borate
Cc1ccc2nc(Cl)c(C)cc2c1
2-chloro-3,6-dimethylquinoline
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cc1cccc(-c2nc3ccc(C)cc3cc2C)c1
2-(3-methylphenyl)-3,6-dimethylquinoline

용매

반응 조건

온도
100°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타After completion of the reaction
  2. 2
    기타the THF and the toluene were removed
  3. 3
    추출The reaction solution was extracted with dichloromethane and water
  4. 4
    workup.DISTILLATIONdistilled under reduced pressure
  5. 5
    기타The resulting residue was purified by silica gel column chromatography
  6. 6
    workup.DISTILLATIONThe eluate was distilled under reduced pressure
  7. 7
    기타The residue was recrystallized from dichloromethane and petroleum ether
  8. 8
    여과filtered

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09023489B2uspto-grants-2015_05