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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1974347Generated: October 27, 2026

Water → 7-(Cyclohexyloxy)-4,6-dinitro-2-(trifluoromethyl)-1H-benzimidazole

https://huagongshe.com/reaction/1974347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCyclohexanolHCID 7966—
ReactantPotassiumHCID 5462222—
Reactant4-Chloro-5,7-dinitro-2-trifluoromethylbenzimidazoleHCID 135677577—
SolventHexamethylphosphoramideHCID 12679—
Product7-(Cyclohexyloxy)-4,6-dinitro-2-(trifluoromethyl)-1H-benzimidazoleHCID 21489355—

Reaction Steps

Cyclohexanol (5.4 grams) and potassium (1.9 grams) were reacted in 50 milliliters of dry hexamethylphosphoric triamide. When reaction had ceased, the solution was stirred and 5 grams of 4-chloro-5,7-dinitro-2-trifluoromethylbenzimidazole were added. Stirring was continued overnight. The reaction mixture was then poured into water, acidified, and extracted with ethyl acetate. The ethyl acetate was then removed by evaporation, and the residue was chromatographed on 300 milliliters of silica gel using benzene as eluant. The benzene was removed by evaporation and the crude product was recrystallized from an aliphatic hydrocarbon fraction boiling at 60°-80° C., to which there had been added a trace of benzene. The resulting 4-cyclohexyloxy-5,7-dinitro-2-trifluoromethylbenzimidazole product melted at 151°-2° C. Its identity was confirmed by NMR and by elemental analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04000295
Source datasetuspto-grants-1976_12
ORD IDord-6e526ddb45724967a7afea5c4772a59b
Source noteuspto-grants-1976_12