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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43430Generated: October 29, 2026

Sodium Acetate → Ethyl 5-ethyl-1H-imidazole-2-carboxylate

https://huagongshe.com/reaction/43430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
Reactant1-aminobutan-2-one HydrochlorideHCID 11607912—
ReactantEthyl imino(methylthio)acetate tetrafluoroborateHCID 86648451—
SolventAcetic AcidHCID 176—
ProductEthyl 5-ethyl-1H-imidazole-2-carboxylateHCID 1499023772.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

Sodium acetate (9.3 g, 113.4 mmol) was added to a solution of 1-amino-butan-2-one hydrochloride (3.41 g, 27.60 mmol) and ethyl imino(methylthio)acetate tetrafluoroborate (7.45 g, 31.84 mmol) synthesized according to the method described in the document (J. Med. Chem., 38, 1995, 2196-2201) in acetic acid (120 mL), and the mixture was stirred at 100° C. for four hours. The reaction solution was concentrated under reduced pressure and then saturated aqueous sodium bicarbonate solution was added to the reaction solution, followed by extraction with ethyl acetate. Then, the organic layer was washed with brine and dried over anhydrous sodium sulfate. Following concentration under reduced pressure, the residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=5/1, 2/1, 1/2) to obtain 3.35 g of the title compound as a pale yellow solid (72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536197B2
Source datasetuspto-grants-2013_09
ORD IDord-6a923d14fb724dcb8fcb490c151050da
Source noteuspto-grants-2013_09