反応 #1973931

ord-66af5de44e80428d975c7c8d950fc2f8

反応方程式

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

溶媒

反応条件

温度
100°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他After completion of the reaction
  2. 2
    その他the solvents were removed
  3. 3
    抽出The reaction mixture was extracted with dichloromethane and water
  4. 4
    workup.DISTILLATIONdistilled under reduced pressure
  5. 5
    その他The resulting residue was purified by silica gel column chromatography
  6. 6
    workup.DISTILLATIONThe eluate was distilled under reduced pressure
  7. 7
    その他The residue was recrystallized from dichloromethane and petroleum ether
  8. 8
    ろ過filtered

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08501328B2uspto-grants-2013_08