تفاعل #657266

ord-000a72fb152148a0ba487b523f8e51a4

معادلة التفاعل

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

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 THF and the toluene were removed
  3. 3
    استخلاصThe reaction solution 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-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.

المصدر

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