Hexafluoro-2-butyne preparation method
A technology of butyne and hexachlorobutadiene, which is applied in the field of preparation of hexafluoro-2-butyne, can solve the problems that it is not suitable for industrialization, 2-butynedioic acid is not easy to obtain, and the raw material price of sulfur tetrafluoride is high. Achieve the effects of easy availability of raw materials, low cost, and less discharge of three wastes
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Embodiment 1
[0034] In a 2L stainless steel reaction kettle with a condenser, add 260g of hexachlorobutadiene, 780g of sulfolane, and 348g of potassium fluoride, raise the temperature to 100°C for reaction, collect the gas phase reaction products, wash with water, wash with alkali, and rectify to obtain hexafluoro- 2-butyne product, the product is sampled and analyzed by gas chromatography, the conversion rate of raw material hexachlorobutadiene is 99%, and the product selectivity is 96%.
Embodiment 2
[0036] Add 260g of hexachlorobutadiene, 1,300g of diethylene glycol dimethyl ether, and 710g of chromium fluoride into a 2L stainless steel reaction kettle with a condenser, heat up to 250°C for reaction, and collect the gaseous reaction products and wash them with water and alkali 1. The hexafluoro-2-butyne product was obtained by rectification, and the product was sampled for gas chromatography analysis. The conversion rate of raw material hexachlorobutadiene was 99%, and the product selectivity was 95%.
Embodiment 3
[0038] Add 260g of hexachlorobutadiene, 800g of N-methylpyrrolidone, and 610g of zinc fluoride into a 2L stainless steel reaction kettle with a condenser, heat up to 150°C for reaction, collect the gas phase reaction products and wash with water, alkali, and rectify The hexafluoro-2-butyne product was obtained, and the product was sampled for gas chromatography analysis. The conversion rate of raw material hexachlorobutadiene was 99%, and the product selectivity was 98.5%.
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