Abstract
Condensation of 2-(4-isopropyl-2-methyl-2-ethyltetrahydro-2H-pyran-4-yl)ethanamine with aromatic aldehydes and ketones and subsequent reduction of the azomethines formed gave secondary amines of the tetrahydropyran series. Reaction of the latter with acetic acid and propionic acid chlorides provided the corresponding amides.
References
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Original Russian Text © N.S. Arutyunyan, R.L. Nazaryan, L.A. Akopyan, N.Z. Akopyan, G.A. Panosyan, G.A. Gevorgyan, 2017, published in Zhurnal Obshchei Khimii, 2017, Vol. 87, No. 7, pp. 1207–1210.
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Arutyunyan, N.S., Nazaryan, R.L., Akopyan, L.A. et al. Synthesis and some transformations of 2-(4-isopropyl-2-methyl-2-ethyltetrahydro-2H-pyran-4-yl)ethanamine. Russ J Gen Chem 87, 1634–1637 (2017). https://doi.org/10.1134/S1070363217070313
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DOI: https://doi.org/10.1134/S1070363217070313