HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1594465Erstellt: 23. Oktober 2026
Difluoro(fluorosulphonyl)acetyl fluoride → CH2=C(CF2Ocf2CF2SO2F)2
https://huagongshe.com/de/reaction/1594465
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Difluoro(fluorosulphonyl)acetyl fluoride | HCID 69614 | — |
| Edukt | Potassium Fluoride | HCID 522689 | — |
| Edukt | CH2=C(CF2Oso2F)2 | HCID 10471472 | — |
| Edukt | HCID 178527443 | HCID 178527443 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Diglyme | HCID 8150 | — |
| Produkt | CH2=C(CF3)CF2Oso2F | HCID 87741755 | — |
| Produkt | CH2=C(CF2Ocf2CF2SO2F)2 | HCID 131726625 | 58% |
Reaktionsschritte
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).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07301059B2 |
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| Quelldatensatz | uspto-grants-2007_11 |
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| ORD ID | ord-2cbcbfce830c4433871f4a401c604c36 |
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| Quellennotiz | uspto-grants-2007_11 |
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