Réaction #554595

ord-d586ef9163c8494087d4dc094c93c9cb

Équation de réaction

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

Conditions de réaction

Température
100°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08623519B2uspto-grants-2014_01