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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075288Generated: November 1, 2026

Acetonitrile → 5-Benzoyl-2-ethyl-4-methylimidazole

https://huagongshe.com/reaction/1075288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant2-Aminobutyric acid methyl esterHCID 151013—
Reactant5-Acetyl-2-ethyl-4-phenylimidazoleHCID 20454139—
Reactant2-hydroxyimino-1-phenylbutane-1,3-dioneHCID 178468376—
SolventEthanolHCID 702—
SolventSodium HydroxideHCID 14798—
Product5-Benzoyl-2-ethyl-4-methylimidazoleHCID 17843762642%

Reaction Steps

An acetonitrile solution (15 ml) of 2-oximino-1-phenyl-1,3-butanedione (1.38 g, 7.22 mmoles) and methyl 2-aminobutyrate (0.85 ml, 7.22 mmol) was refluxed under nitrogen for 26.4 h. After concentrating the cooled reaction mixture, the residue was dissolved in 10 ml of ethanol and 20 ml of 10% aqueous sodium hydroxide. This mixture was refluxed 4.9 h, cooled, then extracted with ethyl acetate. Removal of the solvent in vacuo gave 0.65 g (42% yield) of 5-benzoyl-2-ethyl-4-methylimidazole and 5-acetyl-2-ethyl-4-phenylimidazole (86:14 respectively).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04395547
Source datasetuspto-grants-1983_07
ORD IDord-662abc48ddb34ec983820ef3d9217e88
Source noteuspto-grants-1983_07