Reacción #470394
ord-a3a8d3c2613447acba254d6162d7c5c4
Ecuación de reacción
N1-(2,6-diisopropylphenyl)benzene-1,2-diamine
→
desired product
Rendimiento 59.9%
1-(2,6-diisopropylphenyl)-2-phenyl-1H-benzo[d]imidazole
Rendimiento 59.9%
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Temperaturaunder reflux for 3 hours
- 2TemperaturaThe reaction mixture was heated up again
- 3Temperaturato reflux overnight
- 4OtroAir was bubbled through the reaction
- 5Temperaturawhile reflux
- 6OtroThe solvent was evaporated
- 7workup.DISSOLUTIONThe residue was dissolved in dichloromethane (200 mL)
- 8OtroThe crude product was purified by column chromatography
Procedimiento
N1-(2,6-diisopropylphenyl)benzene-1,2-diamine (8.5 g, 32 mmol) and benzldehyde (3 g, 28.8 mmol) were reacted in acetonitrile (100 ml) under reflux for 3 hours. The reaction mixture was cooled to room temperature. Ferric chloride (0.05 g, 0.28 mmol) was added. The reaction mixture was heated up again to reflux overnight. Air was bubbled through the reaction while reflux. The solvent was evaporated. The residue was dissolved in dichloromethane (200 mL) and ran through a short silica gel plug. The crude product was purified by column chromatography using dichloromethane to 3% of ethyl acetate in dichloromethane. 3.4 g of desired product was obtained.