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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322064Generated: October 30, 2026

Aminoacetaldehyde dimethyl acetal → 2-(3-nitrophenyl)-1H-imidazole

https://huagongshe.com/reaction/322064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
Reactant3-nitro-benzimidic acid methyl esterHCID 12200832—
SolventMethanolHCID 887—
Product2-(3-nitrophenyl)-1H-imidazoleHCID 82100148.7%

Reaction Steps

A stirred solution of methyl 3-nitrobenzimidate (7.57 g) and aminoacetaldehyde dimethylacetal (5.57 g) in methanol (20 ml) is heated under reflux for 24 hours. The cool solution is evaporated, and the residue treated with water (9.5 ml) and conc. hydrochloric acid (21 nil). The mixture is heated (steam bath) for 15 minutes and evaporated under reduced pressure. Water (50 ml) is added to the residue and the insoluble solid filtered and washed with water. The filtrate is neutralized with potassium carbonate solution and the precipitated solid filtered and washed with water. The combined solids are charcoaled and recrystallised from ethanol to give 3.87 g of 2-(3nitrophenyl)imidazole, mp 193-194.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211220B1
Source datasetuspto-grants-2001_04
ORD IDord-c2438538b363415a82764565feb8661b
Source noteuspto-grants-2001_04