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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926951Generated: October 31, 2026

Cumene → (Fluoromethyl)(isopropylphenyl)(p-tolyl)sulfonium tetrafluoroborate

https://huagongshe.com/reaction/926951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCumeneHCID 7406—
ReactantTetrafluoroboric acidHCID 28118—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant1-(Fluoromethylsulfinyl)-4-methylbenzeneHCID 325134—
SolventDiethyl EtherHCID 3283—
Product(Fluoromethyl)(isopropylphenyl)(p-tolyl)sulfonium tetrafluoroborateHCID 87429201—

Reaction Steps

1-((Fluoromethyl)sulfinyl)-4-methylbenzene (738 mg, 4.29 mmol) of example 5 was dissolved in dry diethyl ether (15 mL) under an argon atmosphere. Cumene (0.66 mL, 1.1 eq) was added to the previous solution and then the mixture was cooled to a temperature below −50° C. After stabilizing the temperature, trifluoromethanesulfonic anhydride (0.72 mL, 1 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%, 1.18 mL, 2 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 (2.22 g) after heating at room temperature.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290446B2
Source datasetuspto-grants-2016_03
ORD IDord-4f51eb4394aa4546a92227ec76c76c20
Source noteuspto-grants-2016_03