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

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Abstract

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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Dörr, M., Röckl, J. L., Rein, J., Schollmeyer, D., & Waldvogel, S. R. (2020). Electrochemical C−H Functionalization of (Hetero)Arenes—Optimized by DoE. Chemistry - A European Journal, 26(45), 10195–10198. https://doi.org/10.1002/chem.202001171

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