Reacción #554595

ord-d586ef9163c8494087d4dc094c93c9cb

Ecuación de reacción

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

Condiciones de reacción

Temperatura
100°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroAfter completion of the reaction
  2. 2
    Temperaturato cool to room temperature
  3. 3
    ExtracciónThe reaction mixture was extracted with ether and saturated NH4Cl
  4. 4
    workup.DISTILLATIONThe extract was distilled under reduced pressure
  5. 5
    OtroThe resulting residue was purified by silica gel column chromatography (hexane: EtOAc=5:1)

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08623519B2uspto-grants-2014_01