
Journal of Fluorine Chemistry p. 135 - 144 (1996)
Update date:2022-08-29
Topics:
Cirkva, Vladimir
Polak, Radek
Paleta, Oldrich
Butane-1,4-diol was fluoroalkylated by its photoaddition reactions with hexafluoropropene and perfluoro (propyl vinyl) ether under atmospheric pressure, by which monofluoroalkylated and bis-fluoroalkylated products were obtained. 1,3-Diols were completely unreactive under the conditions. 2,2,2-Trifluoroethanol, tert.butyl alcohol and methyl tert.butyl ether appeared to be inert solvents for the additions while acetonitrile quenched the reactions. The reactivity of perfluoro vinyl ethers was studied ( tested) in their photoaddition reactions with alkanols that were less regioselective (up to 7% rel.of regioisomer) in comparison with hexafluoropropene. Surprisingly, photo-supported base-induced nucleophilic mono-and bis-addition of butane-1,4-diol onto hexafluoropropene was observed in acetonitrile.
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