反应 #1973931

ord-66af5de44e80428d975c7c8d950fc2f8

反应方程式

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

溶剂

反应条件

温度
100°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

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

实验过程

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.

来源

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