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Synthesis and properties of water-soluble 2-aminomethylidene derivatives of 1,3-dicarbonyl compounds

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Abstract

A series of [(2-dimethylamino)ethylamino]methylidene-1,3-dicarbonyl compounds was synthesized for the first time starting from the corresponding 2-ethoxymethylidene derivatives and N,N-dimethylethylenediamine. It was shown that further alkylation of aminomethylidene derivatives with methyl iodide occurs regioselectively at the tertiary nitrogen atom. Quaternization products obtained exhibit high corrosion inhibition of mild steel in hydrochloric acid medium.

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Authors and Affiliations

  1. Postovskii Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, ul. S. Kovalevskoi 22, Moscow, 620990, Russia

    D. N. Bazhin, Yu. S. Kudyakova, T. I. Gorbunova, Ya. V. Burgart, A. Ya. Zapevalov & V. I. Saloutin

Authors
  1. D. N. Bazhin
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  2. Yu. S. Kudyakova
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  3. T. I. Gorbunova
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  4. Ya. V. Burgart
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  5. A. Ya. Zapevalov
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  6. V. I. Saloutin
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Correspondence to D. N. Bazhin.

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Original Russian Text © D.N. Bazhin, Yu.S. Kudyakova, T.I. Gorbunova, Ya.V. Burgart, A.Ya. Zapevalov, V.I. Saloutin, 2013, published in Zhurnal Obshchei Khimii, 2013, Vol. 83, No. 7, pp. 1077–1082.

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Bazhin, D.N., Kudyakova, Y.S., Gorbunova, T.I. et al. Synthesis and properties of water-soluble 2-aminomethylidene derivatives of 1,3-dicarbonyl compounds. Russ J Gen Chem 83, 1330–1335 (2013). https://doi.org/10.1134/S1070363213070050

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  • DOI: https://doi.org/10.1134/S1070363213070050

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