Halogenated hydrocarbons containing fluorine and processes for t

Organic compounds -- part of the class 532-570 series – Organic compounds – Halogen containing

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570132, 570135, 570153, C07C 1908

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active

061569437

ABSTRACT:
Processes are disclosed for producing hydrohaloolefins having the formula CF.sub.2 .dbd.C(CH.sub.2 RF)CF.sub.3, the formula FRCF.dbd.C(CH.sub.2 RF)CF.sub.3 or the formula FRCF.dbd.C(CH.sub.2 RF)(CF.sub.2 RF) wherein each R is a difinctional group of the formula --C.sub.2 F.sub.2 XY-- where X and Y are attached to the same carbon, each X is H, Br, Cl or F and each Y is F or CF.sub.3. The processes involve reacting (CF.sub.3).sub.2 C.dbd.CH.sub.2 or certain olefinic adducts thereof with a second olefm of the formula CF.sub.2 .dbd.CXY in the liquid phase in the presence of a Lewis acid catalyst selected from the group consisting of antimony pentafluoride and aluminum chlorofluoride.
Also disclosed is 1,1,2,2,-tetrafluoro-3,3-bistrifluoromethylcyclobutane and a process for its production which involves reacting (CF.sub.3).sub.2 C.dbd.CH.sub.2 with CF.sub.2 .dbd.CF.sub.2 in the liquid phase in the presence of a Lewis acid catalyst selected from the group consisting of antimony pentafluoride and aluminum chlorofluoride.
Also disclosed are olefins of the formula FRCF.dbd.C(CH.sub.2 RF)CF.sub.3, FRCF.dbd.C(CH.sub.2 RF)(CF.sub.2 RF) or CF.sub.2 .dbd.C(CH.sub.2 R.sup.1 F.)CF.sub.3 (R, X and Y are defined as above) wherein R.sup.1 is --C.sub.2 F.sub.2 X(CF.sub.3)-- where X and (CF.sub.3) are attached to the same carbon or --C.sub.2 F.sub.3 X.sup.1 -- wherein X.sup.1 is H, Br or Cl.

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Krespan et al., Chem. Rev., 96, 3269-3301, 1996.
Snegirev et al., Catalytic and Hydride Reduction of Hexafluoropropylene Dimers, Plenum Publishing Corporation, 2489-2494, 1984.

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