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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033222Generated: October 26, 2026

Ammonia → 1H-benzimidazole-2-carbonitrile

https://huagongshe.com/reaction/1033222

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 numberUS05310747
Source datasetuspto-grants-1994_05
ORD IDord-c2c55a029aa84f47aee5eac07f8ae2a0
Source noteuspto-grants-1994_05