Cargando…

Natural phosphate-supported Cu(ii), an efficient and recyclable catalyst for the synthesis of xanthene and 1,4-disubstituted-1,2,3-triazole derivatives

Cu(NO(3))(2) supported on natural phosphate, Cu(ii)/NP, was prepared by co-precipitation and applied as a heterogeneous catalyst for synthesizing xanthenes (2–3 h, 85–97%) through Knoevenagel–Michael cascade reaction of aromatic aldehydes with 1,3-cyclic diketones in ethanol under refluxing conditio...

Descripción completa

Detalles Bibliográficos
Autores principales: Amini, Abbas, Fallah, Azadeh, Cheng, Chun, Tajbakhsh, Mahmood
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9091919/
https://www.ncbi.nlm.nih.gov/pubmed/35559273
http://dx.doi.org/10.1039/c8ra08260j
_version_ 1784705028906287104
author Amini, Abbas
Fallah, Azadeh
Cheng, Chun
Tajbakhsh, Mahmood
author_facet Amini, Abbas
Fallah, Azadeh
Cheng, Chun
Tajbakhsh, Mahmood
author_sort Amini, Abbas
collection PubMed
description Cu(NO(3))(2) supported on natural phosphate, Cu(ii)/NP, was prepared by co-precipitation and applied as a heterogeneous catalyst for synthesizing xanthenes (2–3 h, 85–97%) through Knoevenagel–Michael cascade reaction of aromatic aldehydes with 1,3-cyclic diketones in ethanol under refluxing conditions. It was further used for regioselective synthesis of 1,4-disubstituted-1,2,3-triazoles (1–25 min, 95–99%) via a three-component reaction between organic halides, aromatic alkynes and sodium azide in methanol at room temperature. The proposed catalyst, Cu(ii)/NP, was characterized using X-ray fluorescence, X-ray diffraction, Fourier-transform infrared spectroscopy, scanning electron microscopy, Brunauer–Emmett–Teller, Barrett–Joyner–Halenda and inductively coupled plasma analyses. Compared to other reports in literature, the reactions took place through a simple co-precipitation, having short reaction time (<3 hours), high reaction yield (>85%), and high recyclability of catalyst (>5 times) without significant decrease in the inherent property and selectivity of catalyst. The proposed protocols provided significant economic and environmental advantages.
format Online
Article
Text
id pubmed-9091919
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-90919192022-05-11 Natural phosphate-supported Cu(ii), an efficient and recyclable catalyst for the synthesis of xanthene and 1,4-disubstituted-1,2,3-triazole derivatives Amini, Abbas Fallah, Azadeh Cheng, Chun Tajbakhsh, Mahmood RSC Adv Chemistry Cu(NO(3))(2) supported on natural phosphate, Cu(ii)/NP, was prepared by co-precipitation and applied as a heterogeneous catalyst for synthesizing xanthenes (2–3 h, 85–97%) through Knoevenagel–Michael cascade reaction of aromatic aldehydes with 1,3-cyclic diketones in ethanol under refluxing conditions. It was further used for regioselective synthesis of 1,4-disubstituted-1,2,3-triazoles (1–25 min, 95–99%) via a three-component reaction between organic halides, aromatic alkynes and sodium azide in methanol at room temperature. The proposed catalyst, Cu(ii)/NP, was characterized using X-ray fluorescence, X-ray diffraction, Fourier-transform infrared spectroscopy, scanning electron microscopy, Brunauer–Emmett–Teller, Barrett–Joyner–Halenda and inductively coupled plasma analyses. Compared to other reports in literature, the reactions took place through a simple co-precipitation, having short reaction time (<3 hours), high reaction yield (>85%), and high recyclability of catalyst (>5 times) without significant decrease in the inherent property and selectivity of catalyst. The proposed protocols provided significant economic and environmental advantages. The Royal Society of Chemistry 2018-12-12 /pmc/articles/PMC9091919/ /pubmed/35559273 http://dx.doi.org/10.1039/c8ra08260j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Amini, Abbas
Fallah, Azadeh
Cheng, Chun
Tajbakhsh, Mahmood
Natural phosphate-supported Cu(ii), an efficient and recyclable catalyst for the synthesis of xanthene and 1,4-disubstituted-1,2,3-triazole derivatives
title Natural phosphate-supported Cu(ii), an efficient and recyclable catalyst for the synthesis of xanthene and 1,4-disubstituted-1,2,3-triazole derivatives
title_full Natural phosphate-supported Cu(ii), an efficient and recyclable catalyst for the synthesis of xanthene and 1,4-disubstituted-1,2,3-triazole derivatives
title_fullStr Natural phosphate-supported Cu(ii), an efficient and recyclable catalyst for the synthesis of xanthene and 1,4-disubstituted-1,2,3-triazole derivatives
title_full_unstemmed Natural phosphate-supported Cu(ii), an efficient and recyclable catalyst for the synthesis of xanthene and 1,4-disubstituted-1,2,3-triazole derivatives
title_short Natural phosphate-supported Cu(ii), an efficient and recyclable catalyst for the synthesis of xanthene and 1,4-disubstituted-1,2,3-triazole derivatives
title_sort natural phosphate-supported cu(ii), an efficient and recyclable catalyst for the synthesis of xanthene and 1,4-disubstituted-1,2,3-triazole derivatives
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9091919/
https://www.ncbi.nlm.nih.gov/pubmed/35559273
http://dx.doi.org/10.1039/c8ra08260j
work_keys_str_mv AT aminiabbas naturalphosphatesupportedcuiianefficientandrecyclablecatalystforthesynthesisofxantheneand14disubstituted123triazolederivatives
AT fallahazadeh naturalphosphatesupportedcuiianefficientandrecyclablecatalystforthesynthesisofxantheneand14disubstituted123triazolederivatives
AT chengchun naturalphosphatesupportedcuiianefficientandrecyclablecatalystforthesynthesisofxantheneand14disubstituted123triazolederivatives
AT tajbakhshmahmood naturalphosphatesupportedcuiianefficientandrecyclablecatalystforthesynthesisofxantheneand14disubstituted123triazolederivatives