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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...

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Autores principales: Valentini, Federica, Brufani, Giulia, Rossini, Gabriele, Campana, Filippo, Lanari, Daniela, Vaccaro, Luigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
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.
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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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