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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795311Generated: October 27, 2026

Water → {4-(Pentafluorophenyl)-2,3,5,6-tetrafluorophenyl}(triflyl)methane

https://huagongshe.com/reaction/1795311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantSodium trifluoromethanesulfinateHCID 23690734—
Reactant4-BromomethylperfluorobiphenylHCID 86591121—
SolventPropionitrileHCID 7854—
Product{4-(Pentafluorophenyl)-2,3,5,6-tetrafluorophenyl}(triflyl)methaneHCID 2218645594%

Reaction Steps

4-(bromomethyl)perfluorobiphenyl (3.68 g, 9 mmol) and sodium trifluoromethane sulfinate (1.69 g, 10.8 mmol) were dissolved in propionitrile (30 mL), and the resultant solution was subjected to heating under reflux for 12 hours. After the reaction, the solution was cooled to room temperature, and water was added for extraction with ethyl acetate. The organic phase was dried with magnesium sulfate, filtrated, and the solvent was removed under reduced pressure. The crude product was purified by silica gel column chromatography (hexane-ethyl acetate=20:1 to 8:1 to 1:1), and the aimed {4-(pentafluorophenyl)-2,3,5,6-tetrafluorophenyl}(triflyl)methane (3.91 g, 8.46 mmol, 94% yield) was isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026409B2
Source datasetuspto-grants-2006_04
ORD IDord-3bedaf32c2f94ed4b92be2c85413d1da
Source noteuspto-grants-2006_04