HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diphenyl Ether → 240482-96-6
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diphenyl Ether | HCID 7583 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Diphenyl sulfoxide | HCID 13679 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 240482-96-6 | HCID 16213833 | 38% |
Reaction Steps
In 100 ml of dichloromethane were dissolved 10.1 g (0.05 mol) of diphenylsulfoxide and 8.51 g (0.05 mol) of diphenyl ether, and 12.6 g (0.06 mol) of trifluoroacetic anhydride was added thereto at 0° C. Then 7.5 g (0.05 mol) of trifluoromethanesulfonic acid was added dropwise thereto at 0 to 5° C., followed by gradually warming to room temperature and reacting for 2 hours with stirring. After completion of the reaction, the reaction solution was washed with 100 ml of water five times and concentrated under reduced pressure, followed by purifying the resulting crude product by a column chromatography to obtain 9.59 g (Yield: 38%) of diphenyl-4-phenoxyphenylsulfonium trifluoromethanesulfonate as a yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07101918B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-a06f3be8d44d47b38d7c49812f147533 |
| Source note | uspto-grants-2006_09 |