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Issue 0, 1968
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Evidence for the formation of a hexahydrotriazine in the condensation of acetaldehyde with methylamine

Abstract

The i.r. and 1H n.m.r. spectra of the product of condensation of acetaldehyde with methylamine are more complex than those expected for the simple azomethine N-ethylidenemethylamine. They are explained in terms of an equilibrium between the monomeric azomethine and two conformers of its cyclic trimer, 1,2,3,4,5,6-hexamethylhexahydro-1,3,5-triazine.

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Article type: Paper
DOI: 10.1039/J39680002591
Citation: J. Chem. Soc. C, 1968,0, 2591-2592
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    Evidence for the formation of a hexahydrotriazine in the condensation of acetaldehyde with methylamine

    G. B. Carter, M. C. McIvor and R. G. J. Miller, J. Chem. Soc. C, 1968, 0, 2591
    DOI: 10.1039/J39680002591

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