Method for preparing 1,2-dibromohexafluoropropane
A technology of dibromohexafluoropropane and hexafluoropropylene, which is applied in the field of 1, can solve the problems of unstable reaction, limited production capacity, and low yield, and achieve the effects of high yield, stable reaction, and environmentally friendly process
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Embodiment 1
[0033] After the mixture of bromine 1.6kg and methanol 60ml was stirred, hexafluoropropylene was continuously fed, and the reaction temperature was 60°C. After 72 hours, the conversion rate of bromine was 20%, and the color of the reaction solution was still purple.
Embodiment 2
[0035] In the mixture of bromine 1.6kg (10mol) and methanol 40ml, add an appropriate amount of catalyst iron ion type perfluorosulfonic acid ion exchange resin, stir, continue to feed 1.35kg (9mol) of hexafluoropropylene for 20 minutes, and the reaction temperature is 25 ° C until The crude product was obtained until the color of the liquid phase changed to light red or colorless. After washing with water and distillation, 1,2-dibromohexafluoropropane is obtained, the purity is 99.95%, the conversion rate of bromine is 99.2%, the selectivity of 1,2-dibromohexafluoropropane is 99.8%, -bromohexafluoropropane not detected.
Embodiment 3
[0037] In the mixture of bromine 1.44kg (9mol) and methanol 40ml, add an appropriate amount of catalyst iron ion type perfluorosulfonic acid ion exchange resin, stir, continue to feed 1.5kg (10mol) of hexafluoropropylene for 20 minutes, and the reaction temperature is 25 ° C until The crude product was obtained until the color of the liquid phase changed to light red or colorless. After washing with water and distillation, 1,2-dibromohexafluoropropane is obtained, the purity is 99.95%, the conversion rate of bromine is 99.4%, the selectivity of 1,2-dibromohexafluoropropane is 99.8%, and -bromohexafluoropropane not detected.
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