Reaktionsgleichung
[Cl:1][C:2]([Cl:10])([Cl:9])[C:3]([C:5](Cl)([Cl:7])[Cl:6])=[O:4].[Sb](F)(F)[F:12]>[Sb](Cl)(Cl)(Cl)(Cl)Cl>[Cl:1][C:2]([Cl:10])([Cl:9])[C:3]([C:5]([Cl:7])([Cl:6])[F:12])=[O:4]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 140 °C
Versuchsvorschrift
A 2-liter round bottom flask equipped with a condenser and mechanical stirrer was charged with 1 liter (6.6 moles) of hexachloroacetone, 411.2 g (2.2 moles) of anhydrous antimony trifluoride and 30 ml of antimony pentachloride. The mixture was heated to 140° C. for a period of one hour then cooled to 0° C. The liquid portion of the reaction was decanted from the salts of the reaction and washed with 5×200 ml portions of 12N HCl dried over MgSO4 and distilled. The fraction boiling at 160°-167° C. afforded 700 g of product as a 3:1 mixture of pentachlorofluoro and tetrachlorodifluoro acetones, respectively, and was used without further purification.
Aufarbeitung
- customA 2-liter round bottom flask equipped with a condenser and mechanical stirrer
- temperaturethen cooled to 0° C
- customThe liquid portion of the reaction was decanted from the salts of the reaction
- washwashed with 5×200 ml portions of 12N HCl
- dry with materialdried over MgSO4
- distillationdistilled
Quellen und Nachweise
- ORD-Eintrag
- ord-e3e64361bc5044fc9f45b4e1227c01cb
- Quelldatensatz
- uspto-grants-1985_12
- Patentnummer
- US04562009
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