تفاعل #657265

ord-eae44b0bdc714add863ffbc050f2673a

معادلة التفاعل

Cc1cccc(OB([O-])[O-])c1
3-Methylphenyl borate
Cc1ccc2nc(Cl)cc(C)c2c1
2-chloro-4,6-dimethylquinoline
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cc1cccc(-c2cc(C)c3ccc(C)cc3n2)c1
2-(3-methylphenyl)-4,7-dimethylquinoline

المذيبات

ظروف التفاعل

درجة الحرارة
100°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

3-Methylphenyl borate (1.3 mmol), 2-chloro-4,6-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 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 2-(3-methylphenyl)-4,7-dimethylquinoline as a solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09023489B2uspto-grants-2015_05