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Electrochemical C−H Functionalization of (Hetero)Arenes—Optimized by DoE

A novel approach towards the activation of different arenes and purines including caffeine and theophylline is presented. The simple, safe and scalable electrochemical synthesis of 1,1,1,3,3,3‐hexafluoroisopropanol (HFIP) aryl ethers was conducted using an easy electrolysis setup with boron‐doped di...

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Autores principales: Dörr, Maurice, Röckl, Johannes L., Rein, Jonas, Schollmeyer, Dieter, Waldvogel, Siegfried R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496267/
https://www.ncbi.nlm.nih.gov/pubmed/32232873
http://dx.doi.org/10.1002/chem.202001171
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author Dörr, Maurice
Röckl, Johannes L.
Rein, Jonas
Schollmeyer, Dieter
Waldvogel, Siegfried R.
author_facet Dörr, Maurice
Röckl, Johannes L.
Rein, Jonas
Schollmeyer, Dieter
Waldvogel, Siegfried R.
author_sort Dörr, Maurice
collection PubMed
description A novel approach towards the activation of different arenes and purines including caffeine and theophylline is presented. The simple, safe and scalable electrochemical synthesis of 1,1,1,3,3,3‐hexafluoroisopropanol (HFIP) aryl ethers was conducted using an easy electrolysis setup with boron‐doped diamond (BDD) electrodes. Good yields up to 59 % were achieved. Triethylamine was used as a base as it forms a highly conductive media with HFIP, making additional supporting electrolytes superfluous. The synthesis was optimized using Design of Experiment (DoE) techniques giving a detailed insight to the significance of the reaction parameters. The mechanism was investigated by cyclic voltammetry (CV). Subsequent transition metal‐catalyzed as well as metal‐free functionalization led to interesting motifs in excellent yields up to 94 %.
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spelling pubmed-74962672020-09-25 Electrochemical C−H Functionalization of (Hetero)Arenes—Optimized by DoE Dörr, Maurice Röckl, Johannes L. Rein, Jonas Schollmeyer, Dieter Waldvogel, Siegfried R. Chemistry Communications A novel approach towards the activation of different arenes and purines including caffeine and theophylline is presented. The simple, safe and scalable electrochemical synthesis of 1,1,1,3,3,3‐hexafluoroisopropanol (HFIP) aryl ethers was conducted using an easy electrolysis setup with boron‐doped diamond (BDD) electrodes. Good yields up to 59 % were achieved. Triethylamine was used as a base as it forms a highly conductive media with HFIP, making additional supporting electrolytes superfluous. The synthesis was optimized using Design of Experiment (DoE) techniques giving a detailed insight to the significance of the reaction parameters. The mechanism was investigated by cyclic voltammetry (CV). Subsequent transition metal‐catalyzed as well as metal‐free functionalization led to interesting motifs in excellent yields up to 94 %. John Wiley and Sons Inc. 2020-06-29 2020-08-12 /pmc/articles/PMC7496267/ /pubmed/32232873 http://dx.doi.org/10.1002/chem.202001171 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Communications
Dörr, Maurice
Röckl, Johannes L.
Rein, Jonas
Schollmeyer, Dieter
Waldvogel, Siegfried R.
Electrochemical C−H Functionalization of (Hetero)Arenes—Optimized by DoE
title Electrochemical C−H Functionalization of (Hetero)Arenes—Optimized by DoE
title_full Electrochemical C−H Functionalization of (Hetero)Arenes—Optimized by DoE
title_fullStr Electrochemical C−H Functionalization of (Hetero)Arenes—Optimized by DoE
title_full_unstemmed Electrochemical C−H Functionalization of (Hetero)Arenes—Optimized by DoE
title_short Electrochemical C−H Functionalization of (Hetero)Arenes—Optimized by DoE
title_sort electrochemical c−h functionalization of (hetero)arenes—optimized by doe
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496267/
https://www.ncbi.nlm.nih.gov/pubmed/32232873
http://dx.doi.org/10.1002/chem.202001171
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