706-78-5Relevant articles and documents
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McBee,Baranauckas
, p. 806 (1949)
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Industrial production method for perfluorocyclopentene
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Paragraph 0032; 0033; 0035; 0036; 0037; 0038, (2018/07/07)
The invention discloses an industrial production method for perfluorocyclopentene, and belongs to the field of fine chemical intermediate synthesis. Cyclopentene, chlorine and pyridine hydrofluoride which are used as raw materials undergo high-temperature chlorination in a solvent sulfolane to obtain octachlorocyclopentene, and the octachlorocyclopentene and pyridine hydrofluoride undergo high-temperature fluorination substitution to obtain the perfluorocyclopentene. Residues obtained after the separation of the product undergo reduced pressure distillation to obtain the solvent sulfolane which can be reused. The method allows the product yield to reach 45-55%, the product content to be more than 99%, the water content to be less than 0.1% and the chloride ion content to be less than 0.1%. The method has the advantages of no pollution in the production process, green production process, high yield, simple steps, facilitation of the reduction of the production cost, high product purity, and facilitation of later application.
Specificity and non-specificity in the sensitized CO2-laser-induced reaction of tetrachloroethene
Earl, Boyd L.,Titus, Richard L.
, p. 1593 - 1602 (2007/10/03)
Previous workers have investigated the reaction of tetrachloroethene using thermal initiation and CO2-laser initiation via sensitizing species. In both instances, the principal product was found to be hexachlorobenzene. One group reported evidence of laser specificity in this reaction, in that BCl3 acted as a sensitizer to produce hexachlorobenzene as the principal product, but SF6 and BBr3 did not. We have found that specificity is highly dependent on reaction conditions. We reproduced the previous results using similar experimental conditions, but under different conditions, we found that the specificity is lost, with all three sensitizers which we used (BCl3, SF6, and SiF4) sensitizing the reaction to produce mainly hexachlorobenzene. There were some differences among the sensitizers, as, for example, the fact that SF6 produced the most nearly pure hexachlorobenzene product.
