HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 492271Erstellt: 24. Oktober 2026
Trifluoroacetyl fluoride → 3,3-Difluoro-3-pentafluoroethoxy-2-trifluoromethylpropene
https://huagongshe.com/de/reaction/492271
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Trifluoroacetyl fluoride | HCID 67716 | — |
| Edukt | Potassium Fluoride | HCID 522689 | — |
| Edukt | CH2=C(CF3)CF2Oso2F | HCID 87741755 | — |
| Lösungsmittel | Diglyme | HCID 8150 | — |
| Produkt | 3,3-Difluoro-3-pentafluoroethoxy-2-trifluoromethylpropene | HCID 85887656 | 31% |
Reaktionsschritte
Trifluoroacetyl fluoride (6 g, 0.051 mole) is bubbled into a mixture of KF (2.4 g, 0.041 mole) and dry diglyme (15 ml). The reaction mixture is stirred at 20° C. for 30 minutes and then CH2═C(CF3)CF2OSO2F (10 g, 0.041 mile) is added gradually. The resulting mixture is stirred at 20° C. for 1 hour. Hexafluoroisobutylene is distilled from the reaction mixture and the residue is poured into water. The organic layer. is separated, washed in turn with aqueous sodium bicarbonate solution and water, and then dried over MgSO4. Distillation gives 3,3-Difluoro-3-pentafluoroethoxy-2-trifluoromethylpropene (CH2═C(CF3)CF2OCF2CF3) (3.5 g, 31% yield, b.pt. 67° C.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07531689B2 |
|---|
| Quelldatensatz | uspto-grants-2009_05 |
|---|
| ORD ID | ord-aaafe8030fd246c1927a22706221032d |
|---|
| Quellennotiz | uspto-grants-2009_05 |
|---|