反応 #554595

ord-d586ef9163c8494087d4dc094c93c9cb

反応方程式

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

実験手順

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.

出典

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