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C3-Alkylation of furfural derivatives by continuous flow homogeneous catalysis
The C3-functionalization of furfural using homogeneous ruthenium catalysts requires the preinstallation of an ortho-directing imine group, as well as high temperatures, which did not allow scaling up, at least under batch conditions. In order to design a safer process, we set out to develop a contin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10167860/ https://www.ncbi.nlm.nih.gov/pubmed/37180458 http://dx.doi.org/10.3762/bjoc.19.43 |
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author | Kinkutu, Grédy Kiala Louis, Catherine Roy, Myriam Blanchard, Juliette Oble, Julie |
author_facet | Kinkutu, Grédy Kiala Louis, Catherine Roy, Myriam Blanchard, Juliette Oble, Julie |
author_sort | Kinkutu, Grédy Kiala |
collection | PubMed |
description | The C3-functionalization of furfural using homogeneous ruthenium catalysts requires the preinstallation of an ortho-directing imine group, as well as high temperatures, which did not allow scaling up, at least under batch conditions. In order to design a safer process, we set out to develop a continuous flow process specifically for the C3-alkylation of furfural (Murai reaction). The transposition of a batch process to a continuous flow process is often costly in terms of time and reagents. Therefore, we chose to proceed in two steps: the reaction conditions were first optimized using a laboratory-built pulsed-flow system to save reagents. The optimized conditions in this pulsed-flow mode were then successfully transferred to a continuous flow reactor. In addition, the versatility of this continuous flow device allowed both steps of the reaction to be carried out, namely the formation of the imine directing group and the C3-functionalization with some vinylsilanes and norbonene. |
format | Online Article Text |
id | pubmed-10167860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-101678602023-05-10 C3-Alkylation of furfural derivatives by continuous flow homogeneous catalysis Kinkutu, Grédy Kiala Louis, Catherine Roy, Myriam Blanchard, Juliette Oble, Julie Beilstein J Org Chem Full Research Paper The C3-functionalization of furfural using homogeneous ruthenium catalysts requires the preinstallation of an ortho-directing imine group, as well as high temperatures, which did not allow scaling up, at least under batch conditions. In order to design a safer process, we set out to develop a continuous flow process specifically for the C3-alkylation of furfural (Murai reaction). The transposition of a batch process to a continuous flow process is often costly in terms of time and reagents. Therefore, we chose to proceed in two steps: the reaction conditions were first optimized using a laboratory-built pulsed-flow system to save reagents. The optimized conditions in this pulsed-flow mode were then successfully transferred to a continuous flow reactor. In addition, the versatility of this continuous flow device allowed both steps of the reaction to be carried out, namely the formation of the imine directing group and the C3-functionalization with some vinylsilanes and norbonene. Beilstein-Institut 2023-05-03 /pmc/articles/PMC10167860/ /pubmed/37180458 http://dx.doi.org/10.3762/bjoc.19.43 Text en Copyright © 2023, Kinkutu et al. https://creativecommons.org/licenses/by/4.0/This is an open access article licensed under the terms of the Beilstein-Institut Open Access License Agreement (https://www.beilstein-journals.org/bjoc/terms/terms), which is identical to the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ). The reuse of material under this license requires that the author(s), source and license are credited. Third-party material in this article could be subject to other licenses (typically indicated in the credit line), and in this case, users are required to obtain permission from the license holder to reuse the material. |
spellingShingle | Full Research Paper Kinkutu, Grédy Kiala Louis, Catherine Roy, Myriam Blanchard, Juliette Oble, Julie C3-Alkylation of furfural derivatives by continuous flow homogeneous catalysis |
title | C3-Alkylation of furfural derivatives by continuous flow homogeneous catalysis |
title_full | C3-Alkylation of furfural derivatives by continuous flow homogeneous catalysis |
title_fullStr | C3-Alkylation of furfural derivatives by continuous flow homogeneous catalysis |
title_full_unstemmed | C3-Alkylation of furfural derivatives by continuous flow homogeneous catalysis |
title_short | C3-Alkylation of furfural derivatives by continuous flow homogeneous catalysis |
title_sort | c3-alkylation of furfural derivatives by continuous flow homogeneous catalysis |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10167860/ https://www.ncbi.nlm.nih.gov/pubmed/37180458 http://dx.doi.org/10.3762/bjoc.19.43 |
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