Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608697Generated: October 29, 2026

Ammonia → 1H-benzimidazole-2-carbonitrile

https://huagongshe.com/reaction/1608697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantBenzimidazole, 2-trichloromethyl-HCID 77133—
SolventEthanolHCID 702—
Product1H-benzimidazole-2-carbonitrileHCID 843858—

Reaction Steps

5.3 Grams of 2-(trichloromethyl)benzimidazole compound [compound (104)] of the formula (XI) in which X is H and Z is OCF2O was suspended in 100 ml of ethanol. The resulting solution was added by drops to 40 ml of a 25% aqueous ammonia at 5° C. After stirring for 1 hour at 5° C. to room temperature, the reaction solution was poured into an ice/conc. hydrochloric acid mixture and extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous sodium sulfate. Removing the solvent from the dried layer by distillation gave 4.0 g of a 2-cyanobenzimidazole compound [compound (iv)] of the formula (II) in which X is H and Z is OCF2O.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05395952
Source datasetuspto-grants-1995_03
ORD IDord-b707cdf3b20a4a6fa15121d498bbcf4b
Source noteuspto-grants-1995_03