Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818642Generated: November 1, 2026

Diethyl Ether → 1,2-Diphenylbenzimidazole

https://huagongshe.com/reaction/1818642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantN-Phenyl-o-phenylenediamineHCID 68297—
SolventDichloromethaneHCID 6344—
Product1,2-DiphenylbenzimidazoleHCID 13766170%

Reaction Conditions

Temperature0 °C

Reaction Steps

40 ml of N-phenyl-1,2-phenylenediamine (7.36 g, 40 mmol) was charged in a 250 ml round bottle, 10 ml of triethylamine was then added, and the mixture was cooled to 0° C. Benzoyl chloride (5.6 g, 40 mmol) was dissolved in 40 ml of dichloromethane and then slowly added to the 250 ml round bottle. The reaction was conducted under a nitrogen atmosphere for 6 hours. After the reaction was complete, ether was added to form precipitate. The solid product was collected by filtration, washed with ether several times, and heated under reduced pressure to form 1,2-diphenyl-1H-benzoimidazole (yield=7.56 g, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601437B2
Source datasetuspto-grants-2009_10
ORD IDord-c4a492a6ef0c4eb5a7bd9fc6c6ef60f4
Source noteuspto-grants-2009_10