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Bromotrimethylsilane as a selective reagent for the synthesis of bromohydrins

Bromotrimethylsilane (TMSBr) is a very efficient reagent in the solvent-free conversion of glycerol into bromohydrins, useful intermediates in the production of fine chemicals. As glycerol is a relevant by-product in biodiesel production, TMSBr has been also tested as a mediator in transesterificati...

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Autores principales: Giomi, Donatella, Salvini, Antonella, Ceccarelli, Jacopo, Brandi, Alberto
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/PMC8697681/
https://www.ncbi.nlm.nih.gov/pubmed/35424012
http://dx.doi.org/10.1039/d1ra01980e
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author Giomi, Donatella
Salvini, Antonella
Ceccarelli, Jacopo
Brandi, Alberto
author_facet Giomi, Donatella
Salvini, Antonella
Ceccarelli, Jacopo
Brandi, Alberto
author_sort Giomi, Donatella
collection PubMed
description Bromotrimethylsilane (TMSBr) is a very efficient reagent in the solvent-free conversion of glycerol into bromohydrins, useful intermediates in the production of fine chemicals. As glycerol is a relevant by-product in biodiesel production, TMSBr has been also tested as a mediator in transesterification in acidic conditions, providing FAME from castor oil in good yields, along with bromohydrins from glycerol. Subsequently the glycerol conversion was optimized and depending on the reaction conditions, glycerol can be selectively converted into α-monobromohydrin (1-MBH) or α,γ-dibromohydrin (1,3-DBH) in very good yields.
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spelling pubmed-86976812022-04-13 Bromotrimethylsilane as a selective reagent for the synthesis of bromohydrins Giomi, Donatella Salvini, Antonella Ceccarelli, Jacopo Brandi, Alberto RSC Adv Chemistry Bromotrimethylsilane (TMSBr) is a very efficient reagent in the solvent-free conversion of glycerol into bromohydrins, useful intermediates in the production of fine chemicals. As glycerol is a relevant by-product in biodiesel production, TMSBr has been also tested as a mediator in transesterification in acidic conditions, providing FAME from castor oil in good yields, along with bromohydrins from glycerol. Subsequently the glycerol conversion was optimized and depending on the reaction conditions, glycerol can be selectively converted into α-monobromohydrin (1-MBH) or α,γ-dibromohydrin (1,3-DBH) in very good yields. The Royal Society of Chemistry 2021-04-16 /pmc/articles/PMC8697681/ /pubmed/35424012 http://dx.doi.org/10.1039/d1ra01980e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Giomi, Donatella
Salvini, Antonella
Ceccarelli, Jacopo
Brandi, Alberto
Bromotrimethylsilane as a selective reagent for the synthesis of bromohydrins
title Bromotrimethylsilane as a selective reagent for the synthesis of bromohydrins
title_full Bromotrimethylsilane as a selective reagent for the synthesis of bromohydrins
title_fullStr Bromotrimethylsilane as a selective reagent for the synthesis of bromohydrins
title_full_unstemmed Bromotrimethylsilane as a selective reagent for the synthesis of bromohydrins
title_short Bromotrimethylsilane as a selective reagent for the synthesis of bromohydrins
title_sort bromotrimethylsilane as a selective reagent for the synthesis of bromohydrins
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697681/
https://www.ncbi.nlm.nih.gov/pubmed/35424012
http://dx.doi.org/10.1039/d1ra01980e
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