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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398733Generated: October 25, 2026

Cyclohexanol → 5-Cyclohexyloxy-2-carbomethoxyaminobenzimidazole

https://huagongshe.com/reaction/2398733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanolHCID 7966—
ReactantSodium hydrideHCID 24758—
Reactant5-Chloro-2-nitroanilineHCID 74218—
ReactantMethyl N-cyanocarbamateHCID 89023—
ReactantHCID 178418361HCID 178418361—
SolventDimethylformamideHCID 6228—
Product5-Cyclohexyloxy-2-carbomethoxyaminobenzimidazoleHCID 20284434—

Reaction Steps

A mixture of cyclohexanol (0.03 mol) in 75 ml. of dry dimethylformamide under nitrogen is agitated while 55% sodium hydride (0.03 mol) in oil is added portionwise. When evolution of hydrogen ceases 2-nitro-5-chloroaniline (0.025 mol) is added with stirring. The mixture is warmed at 75°-80° C. for 1 hour then poured onto 6 volumes of ice slurry. The separated product recrystallized from water to give red crystals of the nitroaminobiphenylether. After hydrogenation and reaction with carbomethoxycyanamide as described above the product, 5-cyclohexyloxy-2-carbomethoxyaminobenzimidazole is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04025638
Source datasetuspto-grants-1977_05
ORD IDord-1c5f0135e69a40848c0e08e99d8c8114
Source noteuspto-grants-1977_05