Reaktion #470387

ord-060636fc728547e29330484f6e5ebe65

Reaktionsgleichung

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

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture was heated up
  2. 2
    Temperaturto reflux for 48 hours
  3. 3
    Sonstigethe solvent was evaporated
  4. 4
    SonstigeThe residue was purified by column chromatography

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08367223B2uspto-grants-2013_02