Reaktion #657267

ord-2e1cee539f1945e0aeb4732e8d56c1a3

Reaktionsgleichung

Cc1cccc(OB([O-])[O-])c1
3-Methylphenyl borate
Cc1ccc2cc(C)c(Cl)nc2c1
2-chloro-3,7-dimethylquinoline
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cc1cccc(-c2nc3cc(C)ccc3cc2C)c1
2-(3-methylphenyl)-3,7-dimethylquinoline

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeAfter completion of the reaction
  2. 2
    Sonstigethe THF and the toluene were removed
  3. 3
    ExtraktionThe reaction mixture was extracted with dichloromethane and water
  4. 4
    workup.DISTILLATIONThe extract was distilled under reduced pressure
  5. 5
    Sonstigepurified by silica gel column chromatography
  6. 6
    workup.DISTILLATIONThe eluate was distilled under reduced pressure
  7. 7
    Sonstigerecrystallized from dichloromethane and petroleum ether
  8. 8
    Sonstigeto obtain a precipitate
  9. 9
    FiltrationThe precipitate was filtered

Vorschrift

3-Methylphenyl borate (1.3 mmol), 2-chloro-3,7-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 mixture was extracted with dichloromethane and water. The extract was distilled under reduced pressure and purified by silica gel column chromatography. The eluate was distilled under reduced pressure and recrystallized from dichloromethane and petroleum ether to obtain a precipitate. The precipitate was filtered to yield 2-(3-methylphenyl)-3,7-dimethylquinoline as a solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09023489B2uspto-grants-2015_05