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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199381Generated: October 29, 2026

P-Xylene → (2,5-Dimethylphenyl)(fluoromethyl)(p-tolyl)sulfonium tetrafluoroborate

https://huagongshe.com/reaction/2199381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-XyleneHCID 7809—
ReactantTetrafluoroboric acidHCID 28118—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant1-(Fluoromethylsulfinyl)-4-methylbenzeneHCID 325134—
SolventDiethyl EtherHCID 3283—
Product(2,5-Dimethylphenyl)(fluoromethyl)(p-tolyl)sulfonium tetrafluoroborateHCID 87429510—

Reaction Steps

1-((fluoromethyl)sulfinyl)-4-methylbenzene (535 mg, 3.38 mmol) of example 5 was dissolved in dry diethyl ether (15 mL) under an argon atmosphere. P-xylene (0.42 mL, 1.0 eq) was added to the previous solution. The mixture was cooled to a temperature below −50° C. After stabilizing the temperature, trifluoromethanesulfonic anhydride (0.52 mL, 0.92 eq) was added slowly maintaining the same temperature. The mixture was stirred, at the same temperature, until the reaction was complete. HBF4 in diethyl ether solution (54%, 1.29 mL, 2.77 eq) was added. The resulting suspension was stirred for 30 minutes. The precipitate tetrafluoroborate salt was isolated by filtration and washed with diethyl ether at 0° C. The desired product was obtained as a slightly yellow oily solid (2.25 g). after heating at room temperature

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359294B2
Source datasetuspto-grants-2016_06
ORD IDord-849685a8f7d4445ab55ae6684483d72a
Source noteuspto-grants-2016_06