Abstract:Passage of C1 to C, haloalkanes through SnC1,-KC1 melts results in halide exchange reactions, alkene formation, and rearrangement (including cyclization) reactions of the organic molecules. Relative reactivities, product distributions and melt composition efects are consistent with a carbonium ion niechanisni in which the melt functions as a halide ion acceptor. Some control of product distribution by choice of Lewis acid character of the melt seems possible.
Die Reaktion der Halogenide (I) in einer Schmelze aus wasserfreiem SnCl2 und KCl führt unter Halogenaustausch zu den Chloriden (II) und unter Dehydrohalogenierung zu den Alkenen (III).
Die Reaktion der Halogenide (I) in einer Schmelze aus wasserfreiem SnCl2 und KCl führt unter Halogenaustausch zu den Chloriden (II) und unter Dehydrohalogenierung zu den Alkenen (III).
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