HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Di(1-naphthyl)phenylsulfonium triflate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Di(1-naphthyl)sulfide | HCID 625448 | — |
| Reactant | Diphenyliodonium trifluoromethanesulfonate | HCID 2737137 | — |
| Catalyst | Cupric benzoate | HCID 164650 | — |
| Solvent | Water | HCID 962 | — |
| Product | Di(1-naphthyl)phenylsulfonium triflate | HCID 22644402 | 90% |
Reaction Steps
Di(1-naphthyl)sulfide (3 g, 0.0104 mole), diphenyliodonium triflate (5.8 g, 0.0135 mole) and copper benzoate (0.08 g, 0.003 mole) are heated without solvent for 3 hours at 120-145° C. under a nitrogen atmosphere. After cooling down, 75 ml ether was added and the mixture vigorously stirred overnight to achive solidification. Filtration and washing with ether yielded a brown solid, which was dissolved in hot water, the solution filtered and the water removed in vacuo. The resulting white solid was stirred in 50 ml ethyl ether for 24 hours, the mixture filtered and the residue washed with ethyl ether, yielding 4.8 g (90%) of the title compound, di-(1-naphthyl)phenylsulfonium triflate. The structure was confirmed by 1H/13C NMR spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06664022B1 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-7272e59530114867b82c8afcbf50b0ba |
| Source note | uspto-grants-2003_12 |