Reaktionsgleichung
[Al+3:1].[Cl-:2].[Cl-].[Cl-].[C:5]([Cl:9])([Cl:8])([Cl:7])[F:6].C(Cl)([Cl:13])(F)F>>[Al+3:1].[Cl-:7].[Cl-:13].[Cl-:2].[C:5]([Cl:9])([Cl:8])([Cl:7])[F:6]Komponenten
4
Reaktionsbedingungen
- Temperatur
- 32.5 °C
Versuchsvorschrift
500 g (3.75 mol) of AlCl3 (Aldrich—99% pure) was stirred mechanically under N2 in a r.b. flask fitted with a −80° C. condenser while 1750 mL (˜2625 g, 19 mol) of CFCl3 was added over a 1.5-hr period. Reaction is very exothermic in the early stages, so addition of CFCl3 was slow at first in order to keep the temperature below 65° C., then rapid. The resulting suspension was stirred an additional 3 hrs while volatiles (CF2Cl2) were allowed to escape through the warmed condenser. The condenser was then replaced with a simple stillhead, and most of the CCl4 was distilled under reduced pressure [mainly bp 38° C. (200 mm)]. Finally, the last traces of volatiles were removed by warming the residual solid to 30-35° C. at 0.05 mm.
Aufarbeitung
- additionwas added over a 1.5-hr period
- customReaction
- customthe temperature below 65° C.
- distillationmost of the CCl4 was distilled under reduced pressure [mainly bp 38° C. (200 mm)]
- customFinally, the last traces of volatiles were removed
Quellen und Nachweise
- ORD-Eintrag
- ord-78ed5966dab4483ea5b63e98c8bf2f39
- Quelldatensatz
- uspto-grants-2001_07
- Patentnummer
- US06262320B1
Verknüpfte Notizen
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