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Single-Step Methylation of Chitosan Using Dimethyl Carbonate as a Green Methylating Agent

N,N,N-Trimethyl chitosan (TMC) is one chitosan derivative that, because of its improved solubility, has been studied for industrial and pharmaceutic applications. Conventional methods for the synthesis of TMC involve the use of highly toxic and harmful reagents, such as methyl iodide and dimethyl su...

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Autores principales: Hemming, Ellen B., Masters, Anthony F., Perosa, Alvise, Selva, Maurizio, Maschmeyer, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6864761/
https://www.ncbi.nlm.nih.gov/pubmed/31690018
http://dx.doi.org/10.3390/molecules24213986
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author Hemming, Ellen B.
Masters, Anthony F.
Perosa, Alvise
Selva, Maurizio
Maschmeyer, Thomas
author_facet Hemming, Ellen B.
Masters, Anthony F.
Perosa, Alvise
Selva, Maurizio
Maschmeyer, Thomas
author_sort Hemming, Ellen B.
collection PubMed
description N,N,N-Trimethyl chitosan (TMC) is one chitosan derivative that, because of its improved solubility, has been studied for industrial and pharmaceutic applications. Conventional methods for the synthesis of TMC involve the use of highly toxic and harmful reagents, such as methyl iodide and dimethyl sulfate (DMS). Although the methylation of dimethylated chitosan to TMC by dimethyl carbonate (DMC, a green and benign methylating agent) was reported recently, it involved a formaldehyde-based procedure. In this paper we report the single-step synthesis of TMC from chitosan using DMC in an ionic liquid. The TMC synthesised was characterised by (1)H NMR spectroscopy and a functionally meaningful degree of quaternisation of 9% was demonstrated after a 12-h reaction time.
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spelling pubmed-68647612019-12-23 Single-Step Methylation of Chitosan Using Dimethyl Carbonate as a Green Methylating Agent Hemming, Ellen B. Masters, Anthony F. Perosa, Alvise Selva, Maurizio Maschmeyer, Thomas Molecules Article N,N,N-Trimethyl chitosan (TMC) is one chitosan derivative that, because of its improved solubility, has been studied for industrial and pharmaceutic applications. Conventional methods for the synthesis of TMC involve the use of highly toxic and harmful reagents, such as methyl iodide and dimethyl sulfate (DMS). Although the methylation of dimethylated chitosan to TMC by dimethyl carbonate (DMC, a green and benign methylating agent) was reported recently, it involved a formaldehyde-based procedure. In this paper we report the single-step synthesis of TMC from chitosan using DMC in an ionic liquid. The TMC synthesised was characterised by (1)H NMR spectroscopy and a functionally meaningful degree of quaternisation of 9% was demonstrated after a 12-h reaction time. MDPI 2019-11-04 /pmc/articles/PMC6864761/ /pubmed/31690018 http://dx.doi.org/10.3390/molecules24213986 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hemming, Ellen B.
Masters, Anthony F.
Perosa, Alvise
Selva, Maurizio
Maschmeyer, Thomas
Single-Step Methylation of Chitosan Using Dimethyl Carbonate as a Green Methylating Agent
title Single-Step Methylation of Chitosan Using Dimethyl Carbonate as a Green Methylating Agent
title_full Single-Step Methylation of Chitosan Using Dimethyl Carbonate as a Green Methylating Agent
title_fullStr Single-Step Methylation of Chitosan Using Dimethyl Carbonate as a Green Methylating Agent
title_full_unstemmed Single-Step Methylation of Chitosan Using Dimethyl Carbonate as a Green Methylating Agent
title_short Single-Step Methylation of Chitosan Using Dimethyl Carbonate as a Green Methylating Agent
title_sort single-step methylation of chitosan using dimethyl carbonate as a green methylating agent
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6864761/
https://www.ncbi.nlm.nih.gov/pubmed/31690018
http://dx.doi.org/10.3390/molecules24213986
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