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Synthesis of Bis‐Thiazolidinones Using Chitosan‐attached Nano‐CuFe2O4 as an Efficient and Retrievable Heterogeneous Catalyst

The preparation of bis‐thiazolidinones has been achieved by a one‐pot condensation reaction of araldehydes, ethylenediamine, and 2‐mercaptoacetic acid in the presence of nano‐CuFe2O4@chitosan under reflux conditions in toluene. The catalyst was characterized by powder X‐ray diffraction (XRD), scanni...

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Bibliographic Details
Published in:Journal of the Chinese Chemical Society (Taipei) 2017-10, Vol.64 (10), p.1213-1219
Main Authors: Safaei‐Ghomi, Javad, Shahbazi‐Alavi, Hossein, Nazemzadeh, Seyed Hadi
Format: Article
Language:English
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Summary:The preparation of bis‐thiazolidinones has been achieved by a one‐pot condensation reaction of araldehydes, ethylenediamine, and 2‐mercaptoacetic acid in the presence of nano‐CuFe2O4@chitosan under reflux conditions in toluene. The catalyst was characterized by powder X‐ray diffraction (XRD), scanning electronic microscopy (SEM), vibrating sample magnetometer (VSM) measurements, thermal gravimetric analysis (TGA), and FT‐IR spectroscopy. This method provides several advantages including excellent yields, wide range of products, reusability of the catalyst, and a low amount of the catalyst. A new method is developed for the synthesis of bis‐thiazolidinones by a one‐pot condensation reaction of araldehydes, ethylenediamine, and 2‐mercaptoacetic acid in the presence of nano‐CuFe2O4@chitosan under reflux conditions in toluene. The catalyst was characterized by powder X‐ray diffraction, scanning electronic microscopy, vibrating sample magnetometer, thermal gravimetric analysis, and FT‐IR spectroscopy.
ISSN:0009-4536
2192-6549
DOI:10.1002/jccs.201700106