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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cumene | HCID 7406 | — |
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 1-(Fluoromethylsulfinyl)-4-methylbenzene | HCID 325134 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (Fluoromethyl)(isopropylphenyl)(p-tolyl)sulfonium tetrafluoroborate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290446B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-4f51eb4394aa4546a92227ec76c76c20 |
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| Source note | uspto-grants-2016_03 |
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