Bieniek Jessica C, Nater Darryl F, Eberwein Sara L, Schollmeyer Dieter, Klein Martin, Waldvogel Siegfried R
Department of Chemistry, Johannes Gutenberg University Mainz, Duesbergweg 10-14, 55128 Mainz, Germany.
Max-Planck-Institute for Chemical Energy Conversion, Stiftstraße 34-36, 45470 Mülheim an der Ruhr, Germany.
JACS Au. 2024 Apr 18;4(6):2188-2196. doi: 10.1021/jacsau.4c00156. eCollection 2024 Jun 24.
Iminophosphoranes are commonly used reagents in organic synthesis and are, therefore, of great interest. An efficient and sustainable iodide-mediated electrochemical synthesis of -sulfonyl iminophosphoranes from readily available phosphines and sulfonamides is reported. This method features low amounts of supporting electrolytes, inexpensive electrode materials, a simple galvanostatic setup, and high conversion rates. The broad applicability could be demonstrated by synthesizing 20 examples in yields up to 90%, having diverse functional groups including chiral moieties and biologically relevant species. Furthermore, electrolysis was performed on a 20 g scale and could be run in repetitive mode by recycling the electrolyte, which illustrates the suitability for large-scale production. A reaction mechanism involving electrochemical mediation by the iodide-based supporting electrolyte is proposed, completely agreeing with all of the results.
亚氨基膦烷是有机合成中常用的试剂,因此备受关注。本文报道了一种高效且可持续的碘化物介导的电化学合成方法,该方法可从易得的膦和磺酰胺合成-磺酰基亚氨基膦烷。此方法具有支持电解质用量少、电极材料廉价、恒电流装置简单以及转化率高的特点。通过合成20个实例,产率高达90%,其中包含多种官能团,包括手性部分和具有生物学相关性的物种,证明了该方法具有广泛的适用性。此外,电解在20克规模上进行,并且可以通过循环电解质以重复模式运行,这表明该方法适用于大规模生产。本文提出了一种基于碘化物的支持电解质进行电化学介导的反应机理,该机理与所有结果完全一致。