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Cu/SiO(2)-Pr-NH-Benz as a novel nanocatalyst for the efficient synthesis of 1,4-disubstituted triazoles and propargyl amine derivatives in an aqueous solution

In this work, an innovative nanocatalyst (Cu/SiO(2)-Pr-NH-Benz) was synthesized and applied to coupling and click reaction in an aqueous solution. This work reports an efficient and straightforward approach for synthesizing diverse propargylamine and 1,2,3-triazole derivatives in excellent yield and...

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Detalles Bibliográficos
Autores principales: Darroudi, Mahdieh, Rouh, Hossein, Hasanzadeh, Mohammad, Shadjou, Nasrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080054/
https://www.ncbi.nlm.nih.gov/pubmed/33948508
http://dx.doi.org/10.1016/j.heliyon.2021.e06766
Descripción
Sumario:In this work, an innovative nanocatalyst (Cu/SiO(2)-Pr-NH-Benz) was synthesized and applied to coupling and click reaction in an aqueous solution. This work reports an efficient and straightforward approach for synthesizing diverse propargylamine and 1,2,3-triazole derivatives in excellent yield and short-time reaction. Also, a novel method involving the Cu NPs supported on the SiO(2) nanocatalyst as a heterogeneous novel catalyst for the “one-pot” three-component A(3)-coupling of aldehyde, amine, and alkynes and “one-pot” click reaction between alkyne, benzyl halide, and sodium azide in the water at room temperature was developed. Significant advantageous such as enhanced catalytic activity with efficient recycling for the one-pot synthesis of 1,4-disubstituted triazoles and propargyl amine derivatives and in green condition were observed. Also, after five successive reactions, the catalytic activity of recycled Cu/SiO(2)-Pr-NH-Benz remained high without significant loss in its intrinsic activity.