Reaktion #1973931

ord-66af5de44e80428d975c7c8d950fc2f8

Reaktionsgleichung

Cc1cccc(OB([O-])[O-])c1
3-Methylphenyl borate
Cc1cc(Cl)nc2ccccc12
2-chloro-4-methylquinoline
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cc1cccc(-c2ncc(C)c3ccccc23)c1
1-(3-methylphenyl)-4-methylisoquinoline

Lösungsmittel

Reaktionsbedingungen

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

Aufarbeitung

  1. 1
    SonstigeAfter completion of the reaction
  2. 2
    Sonstigethe solvents were removed
  3. 3
    ExtraktionThe reaction mixture was extracted with dichloromethane and water
  4. 4
    workup.DISTILLATIONdistilled under reduced pressure
  5. 5
    SonstigeThe resulting residue was purified by silica gel column chromatography
  6. 6
    workup.DISTILLATIONThe eluate was distilled under reduced pressure
  7. 7
    SonstigeThe residue was recrystallized from dichloromethane and petroleum ether
  8. 8
    Filtrationfiltered

Vorschrift

3-Methylphenyl borate (1.3 mmol), 2-chloro-4-methylquinoline (1 mmol), tetrakis(triphenylphosphine) palladium(0) (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 solvents were removed. The reaction mixture 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 1-(3-methylphenyl)-4-methylisoquinoline as a solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08501328B2uspto-grants-2013_08