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POLITAG-M-F as Heterogeneous Organocatalyst for the Waste-Minimized Synthesis of β-Azido Carbonyl Compounds in Batch and under Flow Conditions
[Image: see text] We herein report a waste minimization protocol for the β-azidation of α,β-unsaturated carbonyl compounds using TMSN(3). The selection of the appropriate catalyst (POLITAG-M-F), in combination with the reaction medium, resulted in enhanced catalytic efficiency and a low environmenta...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945162/ https://www.ncbi.nlm.nih.gov/pubmed/36844749 http://dx.doi.org/10.1021/acssuschemeng.2c07213 |
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author | Valentini, Federica Brufani, Giulia Rossini, Gabriele Campana, Filippo Lanari, Daniela Vaccaro, Luigi |
author_facet | Valentini, Federica Brufani, Giulia Rossini, Gabriele Campana, Filippo Lanari, Daniela Vaccaro, Luigi |
author_sort | Valentini, Federica |
collection | PubMed |
description | [Image: see text] We herein report a waste minimization protocol for the β-azidation of α,β-unsaturated carbonyl compounds using TMSN(3). The selection of the appropriate catalyst (POLITAG-M-F), in combination with the reaction medium, resulted in enhanced catalytic efficiency and a low environmental footprint. The thermal and mechanical stability of the polymeric support allowed us to recover the POLITAG-M-F catalyst for up to 10 consecutive runs. The CH(3)CN:H(2)O azeotrope has a 2-fold positive effect on the process, increasing the efficiency of the protocol and minimizing waste generation. Indeed, the azeotropic mixture, used as a reaction medium and for the workup procedure, was recovered by distillation, leading to an easy and environmentally friendly procedure for product isolation in high yield and with a low E-factor. A comprehensive evaluation of the environmental profile was performed by the calculation of different green metrics (AE, RME, MRP, 1/SF) and a comparison with other literature available protocols. A flow protocol was defined to scale-up the process, and up to 65 mmol of substrates were efficiently converted with a productivity of 0.3 mmol/min. |
format | Online Article Text |
id | pubmed-9945162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-99451622023-02-23 POLITAG-M-F as Heterogeneous Organocatalyst for the Waste-Minimized Synthesis of β-Azido Carbonyl Compounds in Batch and under Flow Conditions Valentini, Federica Brufani, Giulia Rossini, Gabriele Campana, Filippo Lanari, Daniela Vaccaro, Luigi ACS Sustain Chem Eng [Image: see text] We herein report a waste minimization protocol for the β-azidation of α,β-unsaturated carbonyl compounds using TMSN(3). The selection of the appropriate catalyst (POLITAG-M-F), in combination with the reaction medium, resulted in enhanced catalytic efficiency and a low environmental footprint. The thermal and mechanical stability of the polymeric support allowed us to recover the POLITAG-M-F catalyst for up to 10 consecutive runs. The CH(3)CN:H(2)O azeotrope has a 2-fold positive effect on the process, increasing the efficiency of the protocol and minimizing waste generation. Indeed, the azeotropic mixture, used as a reaction medium and for the workup procedure, was recovered by distillation, leading to an easy and environmentally friendly procedure for product isolation in high yield and with a low E-factor. A comprehensive evaluation of the environmental profile was performed by the calculation of different green metrics (AE, RME, MRP, 1/SF) and a comparison with other literature available protocols. A flow protocol was defined to scale-up the process, and up to 65 mmol of substrates were efficiently converted with a productivity of 0.3 mmol/min. American Chemical Society 2023-02-08 /pmc/articles/PMC9945162/ /pubmed/36844749 http://dx.doi.org/10.1021/acssuschemeng.2c07213 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Valentini, Federica Brufani, Giulia Rossini, Gabriele Campana, Filippo Lanari, Daniela Vaccaro, Luigi POLITAG-M-F as Heterogeneous Organocatalyst for the Waste-Minimized Synthesis of β-Azido Carbonyl Compounds in Batch and under Flow Conditions |
title | POLITAG-M-F
as Heterogeneous Organocatalyst for the
Waste-Minimized Synthesis of β-Azido Carbonyl Compounds
in Batch and under Flow Conditions |
title_full | POLITAG-M-F
as Heterogeneous Organocatalyst for the
Waste-Minimized Synthesis of β-Azido Carbonyl Compounds
in Batch and under Flow Conditions |
title_fullStr | POLITAG-M-F
as Heterogeneous Organocatalyst for the
Waste-Minimized Synthesis of β-Azido Carbonyl Compounds
in Batch and under Flow Conditions |
title_full_unstemmed | POLITAG-M-F
as Heterogeneous Organocatalyst for the
Waste-Minimized Synthesis of β-Azido Carbonyl Compounds
in Batch and under Flow Conditions |
title_short | POLITAG-M-F
as Heterogeneous Organocatalyst for the
Waste-Minimized Synthesis of β-Azido Carbonyl Compounds
in Batch and under Flow Conditions |
title_sort | politag-m-f
as heterogeneous organocatalyst for the
waste-minimized synthesis of β-azido carbonyl compounds
in batch and under flow conditions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945162/ https://www.ncbi.nlm.nih.gov/pubmed/36844749 http://dx.doi.org/10.1021/acssuschemeng.2c07213 |
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