Bieniek Jessica C, Mashtakov Boris, Schollmeyer Dieter, Waldvogel Siegfried R
Department of Chemistry, Johannes Gutenberg University Mainz, Duesbergweg 10-14, 55128, Mainz, Germany.
Institute of Biological and Chemical Systems - Functional Molecular Systems (IBCS-FMS), Kaiserstraße 12, 76131, Karlsruhe, Germany.
Chemistry. 2024 Feb 1;30(7):e202303388. doi: 10.1002/chem.202303388. Epub 2023 Dec 13.
Electrochemically generated hypervalent iodine(III) species are powerful reagents for oxidative C-N coupling reactions, providing access to valuable N-heterocycles. A new electrocatalytic hypervalent iodine(III)-mediated in-cell synthesis of 1H-N-aryl-3,4-dihydroquinolin-2-ones by dehydrogenative C-N bond formation is presented. Catalytic amounts of the redox mediator, a low supporting electrolyte concentration and recycling of the solvent used make this method a sustainable alternative to electrochemical ex-cell or conventional approaches. Furthermore, inexpensive, readily available electrode materials and a simple galvanostatic set-up are applied. The broad functional group tolerance could be demonstrated by synthesizing 23 examples in yields up to 96 %, with one reaction being performed on a 10-fold higher scale. Based on the obtained results a sound reaction mechanism could be proposed.
电化学产生的高价碘(III)物种是用于氧化C-N偶联反应的强大试剂,可用于合成有价值的N-杂环化合物。本文介绍了一种通过脱氢C-N键形成,以电催化高价碘(III)介导的细胞内合成1H-N-芳基-3,4-二氢喹啉-2-酮的方法。催化量的氧化还原介质、低浓度的支持电解质以及所用溶剂的循环利用,使该方法成为电化学体外或传统方法的可持续替代方案。此外,还应用了廉价、易得的电极材料和简单的恒电流装置。通过合成了23个例子,产率高达96%,其中一个反应的规模扩大了10倍,证明了该方法对广泛官能团的耐受性。基于所得结果,提出了合理的反应机理。