Durch Bromierung ausgelöste Umlagerung tertiärer Allylalkohole: Der Einfluss eines Fluor‐Substituenten auf Reaktionsgeschwindigkeit und Reaktionsverlauf

Rearrangement of Tertiary Allyl Alcohols Induced by Bromination: The Effect of a Fluorine Substituent on the Rate and the Outcome of the Reaction The allyl alcohol bearing a methyl and a t ‐butyl group at the hydroxylated position was found to undergo a rearrangement when treated with bromine (or N ‐bromosuccinimide) in an aqueous medium and to afford a product mixture containing two regioisomeric ketones and one oxirane. Introduction of an additional methyl group or a fluorine atom at the non‐terminal olefinic center led to a more selective discrimination between potential migratory groups. As the result of an exclusive t ‐butyl shift only one product, a ketone, was formed in both cases. Whereas the reaction rate was only slightly affected by the additional methyl group, it was substantially decreased by the fluorine atom.