HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199397Generated: October 29, 2026
1,2,3,4-Tetramethylbenzene → (Bromomethyl)(phenyl)(2,3,4,5-tetramethylphenyl)sulfonium tetrafluoroborate
https://huagongshe.com/reaction/2199397
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2,3,4-Tetramethylbenzene | HCID 10263 | — |
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | Bromomethyl phenyl sulfoxide | HCID 11816834 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (Bromomethyl)(phenyl)(2,3,4,5-tetramethylphenyl)sulfonium tetrafluoroborate | HCID 87429158 | — |
Reaction Steps
Bromomethyl phenyl sulfoxide (1 g, 4.58 mmol) of example 32 was dissolved in dry diethyl ether (30 mL) under an argon atmosphere. 1,2,3,4-tetramethylbenzene (0.678 g, 1.09 eq) was added to the previous solution and then the mixture was cooled to a temperature below −60° C. After stabilizing the temperature, trifluoromethanesulfonic anhydride (0.77 mL, 1 eq) was added slowly, maintaining the same temperature. The mixture was stirred until the reaction was complete. After 3 hours at −60° C., HBF4 in diethyl ether was added (54%, 1.11 mL, 1.75 eq). The resulting suspension was stirred for 30 minutes. The precipitated tetrafluoroborate salt formed was isolated by filtration and dried under vacuum. 1.24 g (62%) of the desired product was obtained as a white solid. mp: 140-142° C.
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-1c5cd80b9d1f448f93b8dc0deecddd0f |
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| Source note | uspto-grants-2016_06 |
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