Reacción #554595
ord-d586ef9163c8494087d4dc094c93c9cb
Ecuación de reacción
tert-butyl-(2-iodo-benzylidene)amine
Propane-2-yl-benzene
triphenylphosphine
sodium carbonate
DMF
→
3-(3,5-dimethylphenyl)-4-methylisoquinoline
Reactantes
Reactivos
Condiciones de reacción
Temperatura
100°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1OtroAfter completion of the reaction
- 2Temperaturato cool to room temperature
- 3ExtracciónThe reaction mixture was extracted with ether and saturated NH4Cl
- 4workup.DISTILLATIONThe extract was distilled under reduced pressure
- 5OtroThe 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.