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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462925Generated: October 27, 2026

1-(1H-Imidazol-1-yl)ethanone → 1-Acetyl-3-[4-(ethoxycarbonylmethoxy)benzyl]imidazolium bromide

https://huagongshe.com/reaction/1462925

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1H-Imidazol-1-yl)ethanoneHCID 17174—
ReactantEthyl 2-[4-(bromomethyl)phenoxy]acetateHCID 12870369—
SolventAcetonitrileHCID 6342—
Product1-Acetyl-3-[4-(ethoxycarbonylmethoxy)benzyl]imidazolium bromideHCID 17847299498.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

2.2 g of 1-acetylimidazole and 5.46 g of ethyl 4-bromomethylphenoxyacetate were added to 5 ml of dry acetonitrile, and the mixture was heated at 60° C. for 2 hours. After completion of the reaction, the solvent was evaporated under reduced pressure. The residue was triturated with an adequate amount of dry diethyl ether and the resulting powder was collected by filtration and dried to obtain 7.5 g of 1-acetyl-3-[4-(ethoxycarbonylmethoxy)benzyl]imidazolium bromide. (98.6% yield). Colorless hygroscopic amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04461905
Source datasetuspto-grants-1984_07
ORD IDord-9f7b7a89136c4505bf9652555cd7e002
Source noteuspto-grants-1984_07