Abstract
The aza-Michael reaction of 3,5-dimethylpyrazole with crotonaldehyde in water involved addition of two aldehyde molecules with formation of 2-[2-(3,5-dimethyl-1H-pyrazol-1-yl)propyl]-6-methyl-1,3-dioxan-4-ol. The latter exists in solution as equilibrium mixture with monocyclic 3-{[3-(3,5-dimethyl-1H-pyrazol-1-yl)-1-hydroxybutyl]oxy}butanal.
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Original Russian Text © H.N. Khachatryan, S.S. Hayotsyan, K.S. Badalyan, A.G. Aivazyan, G.G. Danagulyan, H.S. Attaryan, 2017, published in Zhurnal Organicheskoi Khimii, 2017, Vol. 53, No. 10, pp. 1570–1572.
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Khachatryan, H.N., Hayotsyan, S.S., Badalyan, K.S. et al. Unusual behavior of 3,5-dimethylpyrazole in the aza-Michael reaction with crotonaldehyde in aqueous medium. Russ J Org Chem 53, 1606–1608 (2017). https://doi.org/10.1134/S1070428017100220
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DOI: https://doi.org/10.1134/S1070428017100220