HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454747Generated: October 25, 2026
Dichloromethane → Triphenylsulfonium perfluorooctanesulfonate
https://huagongshe.com/reaction/1454747
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triphenylsulfonium Bromide | HCID 11984010 | — |
| Reactant | Potassium perfluorooctanesulfonate | HCID 23669238 | — |
| Solvent | Water | HCID 962 | — |
| Product | Triphenylsulfonium perfluorooctanesulfonate | HCID 21863781 | — |
Reaction Steps
To a suspension of perfluorooctanesulfonic acid potassium salt (10.76 g, 20.0 mmol) in water (100 mL) at room temperature under nitrogen was added dropwise triphenylsulfonium bromide (6.87 g, 20.0 mmol) over 15 min. After stirring the suspension for 30 min., dichloromethane (100 mL) was added and the biphasic mixture stirred at room temperature for 20 hours. Additional dichloromethane (100 mL) was added and the layers separated. The organic layer was washed with water (3×75 mL) until the washings were neutral (pH 7). After drying (MgSO4), removal of the solvent in vacuum gave a viscous gum which was further dried by heating at 50° C. for 24 hours under vacuum. In this way, triphenylsulfonium perfluorooctanesulfonate was isolated as a pale yellow gummy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07482107B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-f07961b98fea45bda6cbfb01b70f1bd8 |
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| Source note | uspto-grants-2009_01 |
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