反应 #554595

ord-d586ef9163c8494087d4dc094c93c9cb

反应方程式

CC(C)(C)N=Cc1ccccc1I
tert-butyl-(2-iodo-benzylidene)amine
CC(C)c1ccccc1
Propane-2-yl-benzene
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
CN(C)C=O
DMF
Cc1cc(C)cc(-c2ncc3ccccc3c2C)c1
3-(3,5-dimethylphenyl)-4-methylisoquinoline

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
    温度to cool to room temperature
  3. 3
    萃取The reaction mixture was extracted with ether and saturated NH4Cl
  4. 4
    workup.DISTILLATIONThe extract was distilled under reduced pressure
  5. 5
    其他The resulting residue was purified by silica gel column chromatography (hexane: EtOAc=5:1)

实验过程

Propane-2-yl-benzene (100 mmol), acetic acid palladium (2.7 mmol), triphenylphosphine (5 mmol), and sodium carbonate (50 mmol) were put in a dried two-neck round-bottom flask and dissolved in DMF (100 ml). Subsequently, tert-butyl-(2-iodo-benzylidene)amine (50 mmol) was added thereto. The resulting solution was stirred in a bath at 100° C. for 24 hours. After completion of the reaction, the temperature was allowed to cool to room temperature. The reaction mixture was extracted with ether and saturated NH4Cl. The extract was distilled under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane: EtOAc=5:1) to yield 3-(3,5-dimethylphenyl)-4-methylisoquinoline.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08623519B2uspto-grants-2014_01