Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276033Generated: October 30, 2026

Ethanol → 2-Benzyl-5-ethoxycarbonylbenzimidazole

https://huagongshe.com/reaction/276033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthyl 3-nitro-4-phenylacetylaminobenzoateHCID 54219833—
SolventAcetic AcidHCID 176—
Product2-Benzyl-5-ethoxycarbonylbenzimidazoleHCID 1022133374.8%

Reaction Steps

A mixture of 3.60 g of ethyl 3-nitro-4-phenylacetylaminobenzoate, 47 ml of ethanol, 23 ml of acetic acid and 6.4 g of reduced iron was heat-refluxed for 4 hours. The solid material was separated through filtration, and the filtrate was concentrated. To the residue were added 50 ml of ethanol and 5 g of 35% hydrochloric acid. The mixture was stirred for 40 hours while being heat-refluxed. The reaction solution was neutralized with sodium hydrogencarbonate, and was extracted with chloroform. The organic layer was concentrated under reduced pressure, and was purified through silica-gel column chromatography to give 2.30 g of 2-benzyl-5-ethoxycarbonylbenzimidazole (150).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352985B1
Source datasetuspto-grants-2002_03
ORD IDord-32210102b51748b088c707e3108cc102
Source noteuspto-grants-2002_03