Faculty of Chemistry, University of Wrocław, 14 F. Joliot-Curie, 50-383 Wrocław, Poland.
Inorg Chem. 2020 May 18;59(10):6895-6904. doi: 10.1021/acs.inorgchem.0c00310. Epub 2020 Apr 30.
A unique method of bisphenol/bisnaphthol synthesis is being proposed, serendipitously discovered in the course of the careful analysis of an aminophenol methylation reaction. The insightful exploration of the synthesis of N- or O-methylated species, originating from functionalized phenols obtained by a conventional strategy, provided the opportunity to discover an unexpected reaction pathway yielding various bisphenols. Sodium complexes were found to be crucial intermediates in the synthetic scenario. Their formation, which is usually an imperceptive step, was substantial for the productive outcome of functional group protection. Thorough exploration revealed an essential structural motif of aminophenolate, necessary for the successful outcome of the reaction, and also enabled establishing the limitations of the new method. The work demonstrated that a slight change in the perspective and close inspection of the synthetic nuances can answer the important question concerning what a specific target-oriented synthesis strategy is lacking.
本文提出了一种独特的双酚/双萘酚合成方法,该方法是在仔细分析氨基酚甲基化反应的过程中偶然发现的。对 N- 或 O- 甲基化物种的合成进行了有见地的探索,这些物种源于通过传统策略获得的官能化苯酚,为发现产生各种双酚的意外反应途径提供了机会。发现钠离子复合物是合成方案中的关键中间体。它们的形成通常是一个不易察觉的步骤,但对于保护官能团的生产性结果至关重要。彻底的探索揭示了氨基酚盐的一个重要结构基序,这对于反应的成功结果是必要的,并且还能够确定新方法的局限性。该工作表明,稍微改变一下观点并仔细检查合成细节,可以回答一个重要问题,即特定的目标导向合成策略缺少什么。