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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411181Generated: November 4, 2026

Trifluoromethanesulfonic acid → 1-Benzoyl-5,5-dimethylimidazolidin-2-one

https://huagongshe.com/reaction/2411181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Benzoyl-1-(4-methoxybenzyl)-4,4-dimethylimidazolidin-2-oneHCID 71252458—
SolventDichloromethaneHCID 6344—
Product1-Benzoyl-5,5-dimethylimidazolidin-2-oneHCID 7125211345.3%

Reaction Steps

3-Benzoyl-1-(4-methoxybenzyl)-4,4-dimethylimidazolidin-2-one (500 mg) described in Preparation Example 57 was dissolved in dichloromethane (5 mL), trifluoromethanesulfonic acid (0.39 mL) was added, and the mixture was stirred at room temperature for 3 hr. To the reaction mixture was added 5% aqueous sodium hydrogen carbonate solution, the solvent was evaporated, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and the solvent was evaporated. The obtained residue was purified by column chromatography (hexane:ethyl acetate) to give the title compound (146 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-73656e08363748a8839c80050d0edbc5
Source noteuspto-grants-2014_08