Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrafluoroethylene | HCID 8301 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Difluoro(fluorosulphonyl)acetyl fluoride | HCID 69614 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Cfc 113 | HCID 6428 | — |
| Product | FSO2CF2CF2OCF2CF2Br | HCID 13311567 | — |
Reaction Steps
A mixture of 5.8 g potassium fluoride, 60 ml acetonitrile and 12 ml fluorosulfonyl difluoroacetyl fluoride was heated at 80° C. for one hour. The resulting mixture was placed in a stainless steel autoclave and heated at 50° C. for one hour and 80° C. for o ne hour with 16 g bromine and 30 g of tetrafluoroethylene. The reaction mixture was poured into a solution of sodium bisulfite, 50 ml 1,1,2-trichloro-1,2,2-trifluoroethane was added and the mixture was distilled to give a distillate boiling up to 100° C. which contained two layers. The organic layer was separated and distilled to give FSO2CF2CF2OCF2CF2Br, b.p. 106°, confirmed by infrared, nuclear magnetic resonance and mass spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04348310 |
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| Source dataset | uspto-grants-1982_09 |
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| ORD ID | ord-f03b4c884ab0430d9041c32c63044d91 |
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| Source note | uspto-grants-1982_09 |
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