Réaction #554595
ord-d586ef9163c8494087d4dc094c93c9cb
Équation de réaction
tert-butyl-(2-iodo-benzylidene)amine
Propane-2-yl-benzene
triphenylphosphine
sodium carbonate
DMF
→
3-(3,5-dimethylphenyl)-4-methylisoquinoline
Réactifs
Réactifs
Conditions de réaction
Température
100°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1AutreAfter completion of the reaction
- 2Températureto cool to room temperature
- 3ExtractionThe reaction mixture was extracted with ether and saturated NH4Cl
- 4workup.DISTILLATIONThe extract was distilled under reduced pressure
- 5AutreThe 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.