Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268307Generated: October 29, 2026

Benzaldehyde → 1-Methyl-5-nitro-2-styrylimidazole

https://huagongshe.com/reaction/268307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantDimetridazoleHCID 3090—
ReactantDimethyl SulfateHCID 6497—
Reactant2-Methyl-5-nitroimidazoleHCID 12760—
ReactantSodium ethoxideHCID 2723922—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
Product1-Methyl-5-nitro-2-styrylimidazoleHCID 327486—

Reaction Steps

The novel compounds coming within the scope of the generic formula, supra, are readily synthesized starting with commercially available 2-methyl-5-nitroimidazole. This starting compound is allowed to react with a suitable alkylating agent, such as dimethyl sulfate, in a suitable solvent, for example benzene, to yield the comopound identified as 1,2-dimethyl-5-nitroimidazole. This latter compound is in turn allowed to react with benzaldehyde in the presence of a base, for example sodium ethoxide in absolute ethanol, to yield 1-methyl-5-nitro-2-styrylimidazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03947467
Source datasetuspto-grants-1976_03
ORD IDord-3decf4d3246844ab9ff2f46fdd3225b8
Source noteuspto-grants-1976_03