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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164805Generated: November 1, 2026

Hydrochloric Acid → 2-(2-Nitrobenzyl)-imidazole

https://huagongshe.com/reaction/2164805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
ReactantEthyl 2-(2-nitrophenyl)acetimidate hydrochlorideHCID 13344902—
SolventSodium HydroxideHCID 14798—
Product2-(2-Nitrobenzyl)-imidazoleHCID 11206478—

Reaction Steps

Ethanol (2,200 ml) and5,156 g (8.81 moles) of ethyl 2-(2-nitrophenyl)acetimidate hydrochloride are charged into a 22 liter flask. The suspension is stirred under nitrogen at room temperature and 1022.9 g (9.73 moles) of aminoacetaldehyde dimethylacetal are added all at once. The mixture is stirred for 1 hour and 1,693 ml of 12N hydrochloric acid are added all at once to cause a gentle exotherm (to 40°). Heat is then applied and the temperature is maintained at 70°-80° for 30 minutes. The solution is cooled to 20° (ice-water bath) and diluted with 2,700 ml of 10N sodium hydroxide solution to precipitate the product. The suspension is stirred at 10° for 1 hour under nitrogen atmosphere, the solid collected by filtration and washed with 3×2,000 ml of water to give 2-(2-nitrobenzyl)imidazole, m.p. 155°-7°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04507311
Source datasetuspto-grants-1985_03
ORD IDord-2fd0c2ea782b4bcaa761b7cff97eddb4
Source noteuspto-grants-1985_03