HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2913Generated: October 24, 2026
Dichloromethane → Triphenylsulfonium perfluorooctanesulfonate
https://huagongshe.com/en/reaction/2913
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triphenylsulfonium chloride | HCID 61343 | — |
| Reactant | Potassium perfluorooctanesulfonate | HCID 23669238 | — |
| Solvent | Water | HCID 962 | — |
| Product | Triphenylsulfonium perfluorooctanesulfonate | HCID 21863781 | — |
Reaction Steps
To a suspension of perfluorooctanesulfonic acid potassium salt (24.64 g, 46.1 mmol) in water (150 ml) at room temperature under nitrogen was added dropwise triphenylsulfonium chloride (50% aqueous solution, 27.50 g) over 15 minutes. After stirring the suspension for 30 minutes, dichloromethane (75 ml) was added and the mixture stirred at room temperature for 20 hours. Additional dichloromethane (225 ml) was added and the layers separated. The organic layer was washed with water (5×125 ml) until the washings were neutral (pH 7 ). After drying (MgSO4 ), removal of the solvent in vacuo gave a viscous gum which was further dried by heating at 80°-90° C. for 84 hours under vacuum. In this way, triphenylsulfonium perfluorooctanesulfonate was isolated as a glassy solid (30.61 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05731364 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-d1e6e90adf2744bfa6b435f6c7114ace |
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| Source note | uspto-grants-1998_03 |
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