HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexafluoropropylene → Carbon Dioxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexafluoropropylene | HCID 8302 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | Pentafluoroallyl fluorosulphate | HCID 2776028 | — |
| Reactant | Boron | HCID 5462311 | — |
| Product | Carbon Dioxide | HCID 280 | — |
| Product | 1,2,2,2-Tetrafluoroethanesulfonyl fluoride | HCID 160613 | — |
Reaction Steps
The starting material, perfluoroallyl fluorosulfate (FAF), CF2 =CFCF2OSO2F, may be prepared as described in U.S. Pat. No. 4,206,138 to D. C. England. England prepared FAF by reacting hexafluoropropylene with SO3 under anhydrous conditions in the presence of a small amount of a trivalent boron compound such as trimethyl borate at 0°-100° C. A possible byproduct is hexafluoropropylene sultone, ##STR2## which is difficult to separate from FAF by distillation. The sultone in the FAF mixture can be hydrolyzed with ice water to give CF3CFHSO2F+HF+CO2 (gas). This product, CF3CFHSO2F, is also difficult to separate from FAF by distillation, but it does not react with Br2 and can be separated from the Br2 adduct of FAF by distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04567003 |
| Source dataset | uspto-grants-1986_01 |
| ORD ID | ord-b81dc8cf8c2a4abe81b6f5b411605a43 |
| Source note | uspto-grants-1986_01 |