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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546578Generated: October 31, 2026

Methane → 5,5-Dimethyl-3-{4-[(trifluoromethyl)sulfanyl]phenyl}imidazolidine-2,4-dione

https://huagongshe.com/reaction/546578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantTriethylamineHCID 8471—
ReactantDiphosgeneHCID 10426—
Reactant4-((Trifluoromethyl)thio)anilineHCID 123054—
ReactantHCID 86629091HCID 86629091—
SolventTolueneHCID 1140—
Product5,5-Dimethyl-3-{4-[(trifluoromethyl)sulfanyl]phenyl}imidazolidine-2,4-dioneHCID 13268068—

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a solution of 8.5 mL of trichloromethyl chloroformate (diphosgene) in 250 mL of toluene are added 1.8 g of 3S charcoal. To this suspension cooled to −20° C. are added 10 g of 4-trifluoromethylthioaniline dissolved in 160 mL of toluene. The reaction mixture is gradually warmed to room temperature and then refluxed for 4 hours. After cooling to room temperature, a suspension of 9.4 g of dimethylglycine ethyl ester hydrochloride in 90 mL of toluene is added, followed by 38 mL of triethylamine and the reaction mixture is refluxed for 15 hours. After filtering through Celite, the filtrate is concentrated under reduced pressure and the residue is taken up in 200 mL of dichloromethane, washed with three times 100 mL of water, dried over magnesium sulphate, filtered and concentrated under reduced pressure. The residue is then triturated in diethyl ether and the solid formed is filtered off and dried to give 12 g of 5,5-dimethyl-3-{4-[(trifluoromethyl)thio]phenyl}imidazolidine-2,4-dione, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935819B2
Source datasetuspto-grants-2011_05
ORD IDord-d829b3f9db12406881e8a7b79c947fca
Source noteuspto-grants-2011_05