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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164806Generated: November 1, 2026

Hydrochloric Acid → 2-[(1H-Imidazol-2-yl)methyl]aniline

https://huagongshe.com/reaction/2164806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant2-(2-Nitrobenzyl)-imidazoleHCID 11206478—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
Product2-[(1H-Imidazol-2-yl)methyl]anilineHCID 13344903—

Reaction Steps

50% Aqueous ethanol (5,672 ml) and 2,890 g (14.22 moles) of 2-(2-nitrobenzyl)imidazole are charged into a 22 liter flask. The suspension is stirred under nitrogen atmosphere and 2,400 g (42.97 moles) of iron powder (100 mesh) are added all at once. The mixture is then warmed to 70° and a solution of 1.7 ml of 12N hydrochloric acid in 8.3 ml absolute ethanol are added. A vigorous exotherm results and a strong reflux occurs that persists for 1.5 hours. When the exotherm subsides, a mixture of 290 ml of 12N HCl and 1400 ml of absolute ethanol are added over 30 minutes. Heat is applied and the mixture is refluxed for 2 hours, diluted with 6,500 ml of absolute ethanol and adjusted to pH 8-9 with 700 ml of 10N sodium hydroxide. The suspension is stirred for 1 hour and filtered. The cake is washed with 1,000 ml of absolute ethanol, the filtrates are combined and the solvent is removed. The remaining solid is then suspended in 10,000 ml of water, stirred under nitrogen atmosphere for two hours, collected, washed with 2,000 ml of water, and dried to yield 2-(2-aminobenzyl)imidazole, m.p. 153°-155°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04507311
Source datasetuspto-grants-1985_03
ORD IDord-6efd8caa81ae42fda885b3f48bb886cf
Source noteuspto-grants-1985_03