Reaction #1973931

ord-66af5de44e80428d975c7c8d950fc2f8

Reaction equation

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

Solvents

Conditions

Temperature
100°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

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

Procedure

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.

Source

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