HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492277Generated: October 25, 2026
Difluoro(fluorosulphonyl)acetyl fluoride → CH2=C(CF2Ocf2CF2SO2F)2
https://huagongshe.com/reaction/492277
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Difluoro(fluorosulphonyl)acetyl fluoride | HCID 69614 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | CH2=C(CF2Oso2F)2 | HCID 10471472 | — |
| Reactant | HCID 178527443 | HCID 178527443 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | CH2=C(CF3)CF2Oso2F | HCID 87741755 | — |
| Product | CH2=C(CF2Ocf2CF2SO2F)2 | HCID 131726625 | 58% |
Reaction Steps
CH2═C(CF2OSO2F)2 is added gradually to FSO2CF2CF2OK, which is prepared from freshly dried KF (3.9 g, 0.067 mole) and FSO2CF2COF (12 g, 0.067 mole) in dry diglyme (30 ml). The resulting mixture is stirred 3 hours at 20° C. The reaction mixture is poured into water. The organic layer is washed with aqueous sodium bicarbonate, then water, and then dried over MgSO4. Distillation gives CH2═C(CF3)CF2OSO2F (0.5 g) and CH2═C(CF2OCF2CF2SO2F)2 (9 g, 58% yield, b.pt. 95-96° C. at 15 mm Hg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531689B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-daa31aa198fd43f28910e7fc0418ebc5 |
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| Source note | uspto-grants-2009_05 |
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