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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759324Generated: November 1, 2026

Ethanol → HCID 70511180, compound

https://huagongshe.com/reaction/1759324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 13022617HCID 13022617—
ProductHCID 70511180HCID 70511180—

Reaction Steps

3.1 g of 1-benzyl-5-chloro-2-phenyl-4-cyanomethylimidazole, together with 2.1 g of p-toluenesulfonic acid monohydrate, was boiled in 100 ml of ethanol for 10 hours. The reaction solution was evaporated to dryness under reduced pressure, and the residue was dissolved in 50 ml of chloroform, followed by washing with 50 ml each of a 5% aqueous sodium bicarbonate solution and water to evaporate the chloroform layer to dryness under reduced pressure. The residue was chromatographed on a column of 60 g of silica gel, and eluted with chloroform. The fractions of the objective compound were collected and evaporated to dryness under reduced pressure, followed by dissolving the residue in 2 ml of 20% hydrogen chloride-ethanol. Upon addition of 50 ml of ether, there was obtained 1.5 g of ethyl 1-benzyl-5-chloro-2-phenylimidazole-4-acetate hydrochloride as colorless prisms, m.p. 120°-124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04340598
Source datasetuspto-grants-1982_07
ORD IDord-0c772b1268934a9c9ce818f03b84e1cc
Source noteuspto-grants-1982_07