Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Mesitylene | HCID 7947 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Diphenyl sulfoxide | HCID 13679 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 21863651 | HCID 21863651 | 84.3% |
Reaction Steps
In 36.1 g (0.3 mole) of mesitylene was dissolved 6.1 g (0.03 mole) of diphenylsulfoxide, and 12.6 g (0.06 mole) of trifluoroacetic anhydride was poured thereinto under cooling at 5° C. or lower and further 4.5 g (0.03 mole) of trifluoromethane sulfonic acid was added dropwise thereto at −5 to 5° C., followed by allowing a reaction to take place at the same temperature for 2 hours with stirring. Into the resultant was poured 20 ml of n-hexane, followed by separation. This process step series was conducted three times and the resulting crude oily substance was crystallized from a mixture of butyl acetate and isopropyl ether and the crystal was recovered by filtration and dried to give 11.5 g (Yield: 84%) of diphenyl-2,4,6-trimethylphenylsulfonium trifluoromethanesulfonate as white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06723483B1 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-c8cb5a2f9c514d19871231c5fc026a6e |
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| Source note | uspto-grants-2004_04 |
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