HuagongsheHuagongshe Chemistry Print Report · For research reference only
Heptafluorobutyric acid → Triphenylsulfonium heptafluorobutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Heptafluorobutyric acid | HCID 9777 | — |
| Reactant | Sulfonium, triphenyl-, 1,1,1-trifluoromethanesulfonate (1:1) | HCID 11729320 | — |
| Catalyst | Tetramethylammonium chloride | HCID 6379 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Triphenylsulfonium heptafluorobutanoate | HCID 22328343 | 119.2% |
Reaction Steps
In aqueous methanol solution were dissolved 20.6 g (50 mmol) of the resulting triphenylsulfonium trifluoromethanesulfonate, and passed through an activated strong base type anion exchange resin (Amberlite IRA-900 by Organo Corp.). To the elutant solution was added 24.8 g (60 mmol) of heptafluorobutyric acid and allowed reacting with stirring at room temperature for 1 hour. After completion of the reaction, the solvent was removed and the residue was dissolved in 200 ml methylene chloride, washed with water 3 times and concentrated under reduced pressure to give 28.4 g (yield: 84%) of triphenylsulfonium heptafluorobutanoate 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-6837c286a7ce4d37b3d50fd655588b40 |
| Source note | uspto-grants-2005_08 |