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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604238Generated: October 29, 2026

N-Phenyl-o-phenylenediamine → 2-(4-Bromophenyl)-1-phenyl-1H-benzo(d)imidazole

https://huagongshe.com/reaction/604238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Phenyl-o-phenylenediamineHCID 68297—
Reactant4-BromobenzaldehydeHCID 70741—
Product2-(4-Bromophenyl)-1-phenyl-1H-benzo(d)imidazoleHCID 23094070—

Reaction Steps

To a flask containing N-phenyl-o-phenylenediamine (9.21 g, 50 mmol) and 4-bromobenzaldehyde (9.25 g, 50 mmol) was added 50 mL of 20-methoxyethanol. After the mixture was refluxed for 48 h, the volatile was removed under vacuum and the residue was extracted with CH2Cl2. The organic extract was washed with brine, dried over anhydrous MgSO4, filtered and pumped dry. The crude product was purified by column chromatography using a mixture of CH2Cl2 and n-hexane (1:1 by vol.) as the eluent. Analytically pure 2-(4-bromophenyl)-1-phenyl-1H-benzo[d]imidazole was isolated as a white solid in 72% (9.77 g) yield. 1H NMR (400 MHz, CDCl3): δ 7.68 (d, 1 H, J=8.0 Hz), 7.35-7.29 (m, 4 H), 7.24-7.20 (m, 1 H), 7.15-7.02 (m, 7 H). MS (FAB): m/z 348.9 (M+). Anal. calcd. for C19H13BrN2: C, 65.35; H, 3.75; N, 8.02. Found: C, 65.22; H, 3.78; N, 8.01.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910228B2
Source datasetuspto-grants-2011_03
ORD IDord-4da01a4208d34ed490387f466425946d
Source noteuspto-grants-2011_03