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Reaction of Lawesson Reagent with 1,2-(N-Benzyliden)iminoalcohols

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Abstract

Lawesson reagent reacts with 2-(N-benzylidenamino)-1-alkanols in boiling benzene to give 2-(N-benzylidenamino)alkoxy(4′-methoxyphenyl)dithiophosphonates. The primarily formed adducts under the action of methanol eliminate benzylidene fragment to give the corresponding 2-aminoalkoxy(4′-methoxyphenyl)dithiophosphonates.

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Authors and Affiliations

  1. Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center, Russian Academy of Sciences, Kazan, Tatarstan, Russia

    P. I. Gryaznov, O. E. Naumova, D. R. Alimova, D. B. Krivolapov, I. A. Litvinov & V. A. Al'fonsov

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  1. P. I. Gryaznov
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  2. O. E. Naumova
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  3. D. R. Alimova
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  4. D. B. Krivolapov
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  5. I. A. Litvinov
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  6. V. A. Al'fonsov
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__________

Translated from Zhurnal Obshchei Khimii, Vol. 75, No. 11, 2005, pp. 1827–1832.

Original Russian Text Copyright © 2005 by Gryaznov, Naumova, Alimova, Krivolapov, Litvinov, Al'fonsov.

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Gryaznov, P.I., Naumova, O.E., Alimova, D.R. et al. Reaction of Lawesson Reagent with 1,2-(N-Benzyliden)iminoalcohols. Russ J Gen Chem 75, 1744–1749 (2005). https://doi.org/10.1007/s11176-005-0503-8

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  • DOI: https://doi.org/10.1007/s11176-005-0503-8

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