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3-Methoxybutan-2-one as a sustainable bio-based alternative to chlorinated solvents

Methylation of acetoin with dimethyl carbonate was performed in a sustainable one-step process, with improved process mass intensity (PMI) and atom economy compared to previously published methods. The resulting product, 3-methoxybutan-2-one (MO) was successfully evaluated as a bio-based solvent, wh...

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Detalles Bibliográficos
Autores principales: Jin, Saimeng, Byrne, Fergal P., Clark, James H., McElroy, Con Robert, Quinn, Alex, Sherwood, James, Hunt, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044657/
https://www.ncbi.nlm.nih.gov/pubmed/35492443
http://dx.doi.org/10.1039/d1ra07322b
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author Jin, Saimeng
Byrne, Fergal P.
Clark, James H.
McElroy, Con Robert
Quinn, Alex
Sherwood, James
Hunt, Andrew J.
author_facet Jin, Saimeng
Byrne, Fergal P.
Clark, James H.
McElroy, Con Robert
Quinn, Alex
Sherwood, James
Hunt, Andrew J.
author_sort Jin, Saimeng
collection PubMed
description Methylation of acetoin with dimethyl carbonate was performed in a sustainable one-step process, with improved process mass intensity (PMI) and atom economy compared to previously published methods. The resulting product, 3-methoxybutan-2-one (MO) was successfully evaluated as a bio-based solvent, while both Kamlet–Taft solvatochromic parameters and Hansen solubility parameters demonstrate its potential viability in the substitution of chlorinated solvents. MO exhibited a low peroxide forming potential and a negative Ames mutagenicity test and was successfully used as a solvent in a Friedel–Crafts acylation (79% yield compared to 77% in dichloromethane) and for N-alkylations. MO is a renewable oxygenated solvent, with the potential ability to substitute carcinogenic halogenated solvents in some applications.
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spelling pubmed-90446572022-04-28 3-Methoxybutan-2-one as a sustainable bio-based alternative to chlorinated solvents Jin, Saimeng Byrne, Fergal P. Clark, James H. McElroy, Con Robert Quinn, Alex Sherwood, James Hunt, Andrew J. RSC Adv Chemistry Methylation of acetoin with dimethyl carbonate was performed in a sustainable one-step process, with improved process mass intensity (PMI) and atom economy compared to previously published methods. The resulting product, 3-methoxybutan-2-one (MO) was successfully evaluated as a bio-based solvent, while both Kamlet–Taft solvatochromic parameters and Hansen solubility parameters demonstrate its potential viability in the substitution of chlorinated solvents. MO exhibited a low peroxide forming potential and a negative Ames mutagenicity test and was successfully used as a solvent in a Friedel–Crafts acylation (79% yield compared to 77% in dichloromethane) and for N-alkylations. MO is a renewable oxygenated solvent, with the potential ability to substitute carcinogenic halogenated solvents in some applications. The Royal Society of Chemistry 2021-12-10 /pmc/articles/PMC9044657/ /pubmed/35492443 http://dx.doi.org/10.1039/d1ra07322b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Jin, Saimeng
Byrne, Fergal P.
Clark, James H.
McElroy, Con Robert
Quinn, Alex
Sherwood, James
Hunt, Andrew J.
3-Methoxybutan-2-one as a sustainable bio-based alternative to chlorinated solvents
title 3-Methoxybutan-2-one as a sustainable bio-based alternative to chlorinated solvents
title_full 3-Methoxybutan-2-one as a sustainable bio-based alternative to chlorinated solvents
title_fullStr 3-Methoxybutan-2-one as a sustainable bio-based alternative to chlorinated solvents
title_full_unstemmed 3-Methoxybutan-2-one as a sustainable bio-based alternative to chlorinated solvents
title_short 3-Methoxybutan-2-one as a sustainable bio-based alternative to chlorinated solvents
title_sort 3-methoxybutan-2-one as a sustainable bio-based alternative to chlorinated solvents
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044657/
https://www.ncbi.nlm.nih.gov/pubmed/35492443
http://dx.doi.org/10.1039/d1ra07322b
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