Abstract
The condensation of 2-[2-isopropyl-4-(3-methylbutyl)tetrahydropyran-4-yl]ethylamine with aromatic aldehydes followed by reduction gave rise to secondary amines of tetrahydropyrane series. Reactions of the obtained amines with acetyl chloride, succinic and phthalic anhydrides resulted in the corresponding acetamides, succinimide, and phthalimide.
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Arutyunyan, N.S., Akopyan, L.A., Akopyan, N.Z., Gevorgyan, G.A., and Panosyan, G.A., Chem. Heterocycl. Comp., 2010, no. 46, p. 620.
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Original Russian Text © N.S. Arutyunyan, R.L. Nazaryan, R.A. Akopyan, G.A. Gevorgyan, G.A. Panosyan, 2014, published in Zhurnal Obshchei Khimii, 2014, Vol. 84, No. 6, pp. 973–976.
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Arutyunyan, N.S., Nazaryan, R.L., Akopyan, R.A. et al. Synthesis and some transformations of 2-[2-isopropyl-4-(3-methylbutyl)tetrahydropyran-4-yl]-ethylamine. Russ J Gen Chem 84, 1153–1156 (2014). https://doi.org/10.1134/S1070363214060176
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DOI: https://doi.org/10.1134/S1070363214060176