Reacción #470387

ord-060636fc728547e29330484f6e5ebe65

Ecuación de reacción

Nc1ccccc1Nc1ccccc1
N1-phenylbenzene-1,2-diamine
O=Cc1ccccc1
benzaldehyde
c1ccc(-c2nc3ccccc3n2-c2ccccc2)cc1
desired product
Rendimiento 37.0%
c1ccc(-c2nc3ccccc3n2-c2ccccc2)cc1
1,2-diphenyl-1H-benzo[d]imidazole
Rendimiento 37.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe mixture was heated up
  2. 2
    Temperaturato reflux for 48 hours
  3. 3
    Otrothe solvent was evaporated
  4. 4
    OtroThe residue was purified by column chromatography

Procedimiento

N1-phenylbenzene-1,2-diamine (4.15 g, 22 mmol) and benzaldehyde (2.1 g, 20 mmol) were mixed with methoxylethanol (60 ml) in a three-neck flask. The mixture was heated up to reflux for 48 hours. After cooled to room temperature, the solvent was evaporated. The residue was purified by column chromatography using dichloromethane to 5% of ethyl acetate in dichloromethane as eluent. 2 g of desired product was obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08367223B2uspto-grants-2013_02