HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → Sulfonium, triphenyl-, 1,1,1-trifluoromethanesulfonate (1:1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Diphenyl sulfoxide | HCID 13679 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Sulfonium, triphenyl-, 1,1,1-trifluoromethanesulfonate (1:1) | HCID 11729320 | 92% |
Reaction Steps
In 200 ml of benzene were dissolved 21.1 g (0.1 mol) of diphenylsulfoxide, and 42.0 g (0.2 mol) of trifluoroacetic acid anhydride were added dropwise thereto at 0 to 5° C., followed by stirring and stirred at 0 to 5° C. for 30 minutes. And then, 15.0 g (0.1 mol) of trifluoromethane sulfonic acid were added dropwise thereto at 0 to 5° C. and allowed to react with stirring at 0 to 20° C. for 3 hours. After completion of the reaction, 500 ml of n-hexane was poured into the resultant and the obtained oily substance separated by decantation was crystallized from methylene chloride/n-hexane, followed by filtration and drying, to give 37.9 g (yield: 92%) of triphenylsulfonium trifluoromethanesulfonate as a white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06924323B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-76ad00ee7d6644eead5077931a8520a5 |
| Source note | uspto-grants-2005_08 |