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
Participants
| Role | Name | HCID | Charge |
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| Reactant | P-Xylene | HCID 7809 | — |
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 1-(Fluoromethylsulfinyl)-4-methylbenzene | HCID 325134 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (2,5-Dimethylphenyl)(fluoromethyl)(p-tolyl)sulfonium tetrafluoroborate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359294B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-849685a8f7d4445ab55ae6684483d72a |
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| Source note | uspto-grants-2016_06 |
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