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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570735Generated: October 30, 2026

(Trifluoromethyl)benzene → HCID 86685393, compound

https://huagongshe.com/reaction/570735

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Trifluoromethyl)benzeneHCID 7368—
ReactantOxonium, trimethyl-, tetrafluoroborate(1-) (1:1)HCID 2735153—
ReactantHCID 68015322HCID 68015322—
SolventEthyl AcetateHCID 8857—
ProductHCID 86685393HCID 86685393—

Reaction Steps

To a mixture of 2-(ethylsulfanyl)-3-[4-(2,2,2-trifluoroethoxy)phenyl]-3,7-dihydropyrido[3,4-d]pyrimidine-4,8-dione (40 mg) and (trifluoromethyl)benzene (10 ml) was added trimethyloxonium tetrafluoroborate (22 mg) at room temperature, and the reaction mixture was heated under reflux for 3 hr, allowed to be cooled to room temperature, and diluted with ethyl acetate. The reaction mixture was washed successively with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane), and recrystallized from a mixed solvent of ethyl acetate/hexane to give the title compound (16 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023858B2
Source datasetuspto-grants-2015_05
ORD IDord-4c0ddd43bbff4c569b9d3280b6276336
Source noteuspto-grants-2015_05