Hydrofluoric Acid → 4,4,5,5-Tetrachloro-2,2-difluoro-1,3-dioxolane
反応式
[C:1]1(=O)[O:7][C:4]([Cl:6])([Cl:5])[C:3]([Cl:9])([Cl:8])[O:2]1.[FH:11].S(F)(F)(F)[F:13]>>[Cl:8][C:3]1([Cl:9])[C:4]([Cl:6])([Cl:5])[O:7][C:1]([F:13])([F:11])[O:2]1参加物
4
反応条件
- 温度
- 200 °C
実験手順
A 360 mL "Hastelloy" C shaker tube was charged with 113 g (0.5 mole) of tetrachloroethylene carbonate, sealed under nitrogen, cooled in a dry ice acetone mixture, evacuated, flushed with nitrogen, reevacuated and charged with 18 g (0.9 mole) of hydrogen fluoride and 194 g (1.8 mole) of sulfur tetrafluoride. The tube was agitated for 10 hours at 200° C. The tube was next chilled in an ice-water bath and then slowly vented to remove the excess SF4 and HF. The product was dumped from the tube into wet ice and allowed to stand a day. The organic phase was separated from the aqueous phase in a polyethylene separatory funnel, then stirred with a 30% aqueous solution of potassium carbonate to neutralize free acid. The product was dried over potassium carbonate and distilled at a reduced pressure. It boils at 126° C. at atmospheric pressure. The best yield of 4,4,5,5-tetrachloro-2,2,-difluoro-1,3-dioxolane was 73%. Infrared and nuclear magnetic resonance (NMR) spectra support the chemical structure (4) of this dioxolane.