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A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones

The acylation of the acetonitrile anion with lactones and esters in ethereal solvents was successfully exploited using inexpensive KOt-Bu to obtain a variety of β-ketonitriles and trifunctionalized building blocks, including useful O-unprotected diols. It was discovered that lactones react to produc...

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Autores principales: Pienaar, Daniel P, Butsi, Kamogelo R, Rousseau, Amanda L, Brady, Dean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902896/
https://www.ncbi.nlm.nih.gov/pubmed/31839839
http://dx.doi.org/10.3762/bjoc.15.287
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author Pienaar, Daniel P
Butsi, Kamogelo R
Rousseau, Amanda L
Brady, Dean
author_facet Pienaar, Daniel P
Butsi, Kamogelo R
Rousseau, Amanda L
Brady, Dean
author_sort Pienaar, Daniel P
collection PubMed
description The acylation of the acetonitrile anion with lactones and esters in ethereal solvents was successfully exploited using inexpensive KOt-Bu to obtain a variety of β-ketonitriles and trifunctionalized building blocks, including useful O-unprotected diols. It was discovered that lactones react to produce the corresponding derivatized cyclic hemiketals. Furthermore, the addition of a catalytic amount of isopropanol, or 18-crown-6, was necessary to facilitate the reaction and to reduce side-product formation under ambient conditions.
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spelling pubmed-69028962019-12-13 A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones Pienaar, Daniel P Butsi, Kamogelo R Rousseau, Amanda L Brady, Dean Beilstein J Org Chem Letter The acylation of the acetonitrile anion with lactones and esters in ethereal solvents was successfully exploited using inexpensive KOt-Bu to obtain a variety of β-ketonitriles and trifunctionalized building blocks, including useful O-unprotected diols. It was discovered that lactones react to produce the corresponding derivatized cyclic hemiketals. Furthermore, the addition of a catalytic amount of isopropanol, or 18-crown-6, was necessary to facilitate the reaction and to reduce side-product formation under ambient conditions. Beilstein-Institut 2019-12-06 /pmc/articles/PMC6902896/ /pubmed/31839839 http://dx.doi.org/10.3762/bjoc.15.287 Text en Copyright © 2019, Pienaar et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Letter
Pienaar, Daniel P
Butsi, Kamogelo R
Rousseau, Amanda L
Brady, Dean
A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones
title A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones
title_full A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones
title_fullStr A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones
title_full_unstemmed A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones
title_short A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones
title_sort green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902896/
https://www.ncbi.nlm.nih.gov/pubmed/31839839
http://dx.doi.org/10.3762/bjoc.15.287
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