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