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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411179Generated: November 4, 2026

3-Benzoyl-1-(4-methoxybenzyl)-4-methylimidazolidin-2-one → 1-Benzoyl-5-methylimidazolidin-2-one

https://huagongshe.com/reaction/2411179

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Benzoyl-1-(4-methoxybenzyl)-4-methylimidazolidin-2-oneHCID 71252150—
SolventTrifluoroacetic acidHCID 6422—
Product1-Benzoyl-5-methylimidazolidin-2-oneHCID 7125275597.5%

Reaction Steps

3-Benzoyl-1-(4-methoxybenzyl)-4-methylimidazolidin-2-one (220 mg) described in Preparation Example 55 was dissolved in trifluoroacetic acid (2 mL), and the mixture was stirred for 4 hr under heated reflux. The solvent was evaporated from the reaction mixture, 5% aqueous sodium hydrogen carbonate solution was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with 5% aqueous sodium hydrogen carbonate solution and saturated brine, and the solvent was evaporated. The obtained residue was purified by column chromatography (hexane:ethyl acetate) to give the title compound (135 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-b112b17ff10c407087f9098365c5bcda
Source noteuspto-grants-2014_08