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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398166Generated: October 29, 2026

Ethyl Acetate → Methyl 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzoate

https://huagongshe.com/reaction/1398166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium BicarbonateHCID 516892—
ReactantAmmonium AcetateHCID 517165—
ReactantMethyl 4-[formyl-(2-oxopropyl)amino]-3-methoxybenzoateHCID 86602464—
SolventAcetic AcidHCID 176—
ProductMethyl 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzoateHCID 2728244352.9%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of methyl 4-[formyl(2-oxopropyl)amino]-3-methoxybenzoate (32.6 g) and ammonium acetate (47.5 g) in acetic acid (65.6 mL) was stirred at 140° C. for 1 hr. After completion of the reaction, ethyl acetate and saturated aqueous sodium hydrogen carbonate solution were added under ice-cooling, and the organic layer was separated. To the aqueous layer was added ethyl acetate, and the organic layer was separated. The organic layers were combined, washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (methanol/ethyl acetate/hexane) to give the title compound (16.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901309B2
Source datasetuspto-grants-2014_12
ORD IDord-83eec42e91884b32a63ec8e9712e1a11
Source noteuspto-grants-2014_12