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Synthesis and structural characterization of β -cyclodextrin butenate

β-cyclodextrin butenate was synthesized by using N, N’-Carbonyldiimidazole (CDI) activating reagent and 4-Dimethylaminopyridine (DMAP) as catalyst. The best preparation condition of β-CD butenate was described as below: reaction temperature was 25°C, concentration of 2-butenoic acid was 450 mmol/L,...

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Autores principales: Li, Yong-Fu, Tian, Zhu-Xi, Shi, Bin, He, Yang-Bo, Long, Ming-Xiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142337/
https://www.ncbi.nlm.nih.gov/pubmed/37125223
http://dx.doi.org/10.1080/15685551.2023.2205741
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author Li, Yong-Fu
Tian, Zhu-Xi
Shi, Bin
He, Yang-Bo
Long, Ming-Xiu
author_facet Li, Yong-Fu
Tian, Zhu-Xi
Shi, Bin
He, Yang-Bo
Long, Ming-Xiu
author_sort Li, Yong-Fu
collection PubMed
description β-cyclodextrin butenate was synthesized by using N, N’-Carbonyldiimidazole (CDI) activating reagent and 4-Dimethylaminopyridine (DMAP) as catalyst. The best preparation condition of β-CD butenate was described as below: reaction temperature was 25°C, concentration of 2-butenoic acid was 450 mmol/L, concentration of DMAP was 12.5 mmol/L and reaction time was 20 minutes and at this condition the yield of β-CD butenate was 0.83 mmol/g. According to the results of FT-IR spectrum, NMR spectroscopy and HPLC-QTof-mass spectrum of β-CD butenate, there were four types β-CD butenate synthesized, which were β-CD-2-butenoic acid monoester, β-CD-2-butenoic acid diester, β-CD-2-butenoic acid triester and β-CD-2-butenoic acid tetraester, respectively.
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spelling pubmed-101423372023-04-29 Synthesis and structural characterization of β -cyclodextrin butenate Li, Yong-Fu Tian, Zhu-Xi Shi, Bin He, Yang-Bo Long, Ming-Xiu Des Monomers Polym Full Length Article β-cyclodextrin butenate was synthesized by using N, N’-Carbonyldiimidazole (CDI) activating reagent and 4-Dimethylaminopyridine (DMAP) as catalyst. The best preparation condition of β-CD butenate was described as below: reaction temperature was 25°C, concentration of 2-butenoic acid was 450 mmol/L, concentration of DMAP was 12.5 mmol/L and reaction time was 20 minutes and at this condition the yield of β-CD butenate was 0.83 mmol/g. According to the results of FT-IR spectrum, NMR spectroscopy and HPLC-QTof-mass spectrum of β-CD butenate, there were four types β-CD butenate synthesized, which were β-CD-2-butenoic acid monoester, β-CD-2-butenoic acid diester, β-CD-2-butenoic acid triester and β-CD-2-butenoic acid tetraester, respectively. Taylor & Francis 2023-04-26 /pmc/articles/PMC10142337/ /pubmed/37125223 http://dx.doi.org/10.1080/15685551.2023.2205741 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Full Length Article
Li, Yong-Fu
Tian, Zhu-Xi
Shi, Bin
He, Yang-Bo
Long, Ming-Xiu
Synthesis and structural characterization of β -cyclodextrin butenate
title Synthesis and structural characterization of β -cyclodextrin butenate
title_full Synthesis and structural characterization of β -cyclodextrin butenate
title_fullStr Synthesis and structural characterization of β -cyclodextrin butenate
title_full_unstemmed Synthesis and structural characterization of β -cyclodextrin butenate
title_short Synthesis and structural characterization of β -cyclodextrin butenate
title_sort synthesis and structural characterization of β -cyclodextrin butenate
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142337/
https://www.ncbi.nlm.nih.gov/pubmed/37125223
http://dx.doi.org/10.1080/15685551.2023.2205741
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