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Synthesis of N,N-Diethylhydrazine and Its Reactions with Carboxylic Acids and Alkyl Halides

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Abstract

N,N-Diethylhydrazine was synthesized by a modified procedure via nitrosation of diethylamine, followed by reduction of the resulting N-nitrosodiethylamine with zinc amalgam in a hydrochloric acid medium. Reactions of N, N-diethylhydrazine with carboxylic acids and alkyl halides resulted in formation of the corresponding hydrazinium salts.

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Authors and Affiliations

  1. Mirzo Ulugbek National University of Uzbekistan, Vuzgorodok, Uzbekistan

    K. N. Akhmedov, Kh. S. Tadzhimukhamedov & U. Ch. Akhmedov

  2. Mirzo Ulugbek National University of Uzbekistan, Tashkent, Uzbekistan

    K. N. Akhmedov, Kh. S. Tadzhimukhamedov & U. Ch. Akhmedov

Authors
  1. K. N. Akhmedov
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  2. Kh. S. Tadzhimukhamedov
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  3. U. Ch. Akhmedov
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Translated from Zhurnal Obshchei Khimii, Vol. 75, No. 11, 2005, pp. 1802–1805.

Original Russian Text Copyright © 2005 by K. Akhmedov, Tadzhimukhamedov, U. Akhmedov.

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Akhmedov, K.N., Tadzhimukhamedov, K.S. & Akhmedov, U.C. Synthesis of N,N-Diethylhydrazine and Its Reactions with Carboxylic Acids and Alkyl Halides. Russ J Gen Chem 75, 1720–1722 (2005). https://doi.org/10.1007/s11176-005-0499-0

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  • DOI: https://doi.org/10.1007/s11176-005-0499-0

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