Abstract
It is shown that in the reaction of 2-vinylpyridinium quaternary salts with methylammonium sulfite under isomerization recyclization conditions a water molecule adds initially to the double bond of the vinyl substituents, after which the resulting carbinols undergo recyclization to N-alkylaniline derivatives. The reaction is accompanied by a parallel process involving dealkylation of the pyridine ring.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 229–232, February, 1982.
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Stupnikova, T.V., Kalafat, V.N., Klyuev, N.A. et al. Recyclization of 2-vinylpyridinium quaternary salts. Chem Heterocycl Compd 18, 179–182 (1982). https://doi.org/10.1007/BF00512964
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DOI: https://doi.org/10.1007/BF00512964