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Condensation Products of Aldehydes with Phenylthiazolidine Obtained from (1,2-Dibromoethyl)benzene

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Abstract

3-Amino-5-phenyl-1,3-thiazolidin-2-iminium bromide was synthesized for the first time by reaction of (1,2-dibromoethyl)benzene with thiosemicarbazide hydrochloride. Its condensation with aromatic aldehydes afforded the corresponding Schiff bases. The structure of the isolated compounds was confirmed by 1H and 13C NMR spectroscopy.

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Authors and Affiliations

  1. Baku State University, 1148, Baku, Azerbaijan

    G. Sh. Duruskari, A. R. Asgarova, Kh. N. Aliyeva, S. A. Musayeva & A. M. Maharramov

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  1. G. Sh. Duruskari
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  2. A. R. Asgarova
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  3. Kh. N. Aliyeva
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  4. S. A. Musayeva
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  5. A. M. Maharramov
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Correspondence to G. Sh. Duruskari.

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Duruskari, G.S., Asgarova, A.R., Aliyeva, K.N. et al. Condensation Products of Aldehydes with Phenylthiazolidine Obtained from (1,2-Dibromoethyl)benzene. Russ J Org Chem 56, 712–715 (2020). https://doi.org/10.1134/S1070428020040223

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  • DOI: https://doi.org/10.1134/S1070428020040223

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