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Synthesis of a new series of 2-hydroxy-5-iodo-N’-(1-arylethylidene)benzohydrazides using a deep eutectic solvent as solvent/catalyst under sonication

We report here the preparation of 2-hydroxy-5-iodo-N’-(1-arylethylidene)benzohydrazide compounds in good to excellent yields (83–98%) within a short reaction time (10–15 min), through a clean and efficient procedure. Seventeen new compounds were synthesized and fully characterized by FT-IR, NMR, and...

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Detalles Bibliográficos
Autores principales: Nguyen, The Thai, Nguyen, Cong Tien, Tran, Phuong Hoang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6726719/
https://www.ncbi.nlm.nih.gov/pubmed/31508526
http://dx.doi.org/10.1016/j.heliyon.2019.e02353
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author Nguyen, The Thai
Nguyen, Cong Tien
Tran, Phuong Hoang
author_facet Nguyen, The Thai
Nguyen, Cong Tien
Tran, Phuong Hoang
author_sort Nguyen, The Thai
collection PubMed
description We report here the preparation of 2-hydroxy-5-iodo-N’-(1-arylethylidene)benzohydrazide compounds in good to excellent yields (83–98%) within a short reaction time (10–15 min), through a clean and efficient procedure. Seventeen new compounds were synthesized and fully characterized by FT-IR, NMR, and HRMS. The deep eutectic solvent can be recovered easily by phase extraction and can be reused up to several times without any significant loss of catalytic activity. Additionally, the method has a wide substrate scope and provides an accessible route for the large-scale direct synthesis of 2-hydroxy-5-iodo-N’-(1-arylethylidene)benzohydrazides.
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spelling pubmed-67267192019-09-10 Synthesis of a new series of 2-hydroxy-5-iodo-N’-(1-arylethylidene)benzohydrazides using a deep eutectic solvent as solvent/catalyst under sonication Nguyen, The Thai Nguyen, Cong Tien Tran, Phuong Hoang Heliyon Article We report here the preparation of 2-hydroxy-5-iodo-N’-(1-arylethylidene)benzohydrazide compounds in good to excellent yields (83–98%) within a short reaction time (10–15 min), through a clean and efficient procedure. Seventeen new compounds were synthesized and fully characterized by FT-IR, NMR, and HRMS. The deep eutectic solvent can be recovered easily by phase extraction and can be reused up to several times without any significant loss of catalytic activity. Additionally, the method has a wide substrate scope and provides an accessible route for the large-scale direct synthesis of 2-hydroxy-5-iodo-N’-(1-arylethylidene)benzohydrazides. Elsevier 2019-08-31 /pmc/articles/PMC6726719/ /pubmed/31508526 http://dx.doi.org/10.1016/j.heliyon.2019.e02353 Text en © 2019 Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Nguyen, The Thai
Nguyen, Cong Tien
Tran, Phuong Hoang
Synthesis of a new series of 2-hydroxy-5-iodo-N’-(1-arylethylidene)benzohydrazides using a deep eutectic solvent as solvent/catalyst under sonication
title Synthesis of a new series of 2-hydroxy-5-iodo-N’-(1-arylethylidene)benzohydrazides using a deep eutectic solvent as solvent/catalyst under sonication
title_full Synthesis of a new series of 2-hydroxy-5-iodo-N’-(1-arylethylidene)benzohydrazides using a deep eutectic solvent as solvent/catalyst under sonication
title_fullStr Synthesis of a new series of 2-hydroxy-5-iodo-N’-(1-arylethylidene)benzohydrazides using a deep eutectic solvent as solvent/catalyst under sonication
title_full_unstemmed Synthesis of a new series of 2-hydroxy-5-iodo-N’-(1-arylethylidene)benzohydrazides using a deep eutectic solvent as solvent/catalyst under sonication
title_short Synthesis of a new series of 2-hydroxy-5-iodo-N’-(1-arylethylidene)benzohydrazides using a deep eutectic solvent as solvent/catalyst under sonication
title_sort synthesis of a new series of 2-hydroxy-5-iodo-n’-(1-arylethylidene)benzohydrazides using a deep eutectic solvent as solvent/catalyst under sonication
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6726719/
https://www.ncbi.nlm.nih.gov/pubmed/31508526
http://dx.doi.org/10.1016/j.heliyon.2019.e02353
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