HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2914Generated: October 26, 2026
Dichloromethane → Triphenylsulfonium 4-trifluoromethylbenzenesulfonate
https://huagongshe.com/reaction/2914
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Triphenylsulfonium chloride | HCID 61343 | — |
| Reactant | 4-(Trifluoromethyl)benzenesulfonyl chloride | HCID 2777399 | — |
| Solvent | Water | HCID 962 | — |
| Product | Triphenylsulfonium 4-trifluoromethylbenzenesulfonate | HCID 22057398 | — |
Reaction Steps
A suspension of 4-trifluoromethylbenzenesulfonyl chloride (20.53 g, 83.9 mmol) in water (150 ml) containing sodium carbonate (9.43 g, 88.10 mmol) was heated at reflux for 22 hours. After cooling to room temperature, triphenylsulfonium chloride (50% aqueous solution, 50.00 g) was added over 15 minutes. After stirring the biphasic mixture for 30 minutes, dichloromethane (300 ml) was added and the mixture stirred at room temperature for 20 hours. The layers were separated and the organic layer washed with water (7×150 ml) until the washings were neutral (pH 7 ). After drying (MgSO4 ), removal of the solvent in vacuo gave a pale yellow foam which was further dried by heating at 80°-100° C. for 108 hours under vacuum. In this way, triphenylsulfonium 4 -trifluoromethylbenzenesulfonate was isolated as a pale yellow glass (36.77 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-36355329f50b4fba91d75f1d3bd8c47f |
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| Source note | uspto-grants-1998_03 |
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