首页> 外文期刊>The Journal of Organic Chemistry >Visible Light-Mediated (Hetero)aryl Amination Using Ni(II) Salts and Photoredox Catalysis in Flow: A Synthesis of Tetracaine
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Visible Light-Mediated (Hetero)aryl Amination Using Ni(II) Salts and Photoredox Catalysis in Flow: A Synthesis of Tetracaine

机译:使用Ni(II)盐的可见光介导(杂)芳基胺化,流动的催化和光毒剂催化:四胞胎的合成

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摘要

We report a visible light-mediated flow process for C-N cross-coupling of (hetero)aryl halides with a variety of amine coupling partners through the use of a photoredox/nickel dual catalyst system. Compared to the method in batch, this flow process enables a broader substrate scope, including less-activated (hetero)aryl bromides and electron-deficient (hetero)aryl chlorides, and significantly reduced reaction times (10 to 100 min). Furthermore, scale up of the reaction, demonstrated through the synthesis of tetracaine, is easily achieved, delivering the C-N cross-coupled products in consistently high yield of 84% on up to a 10 mmol scale.
机译:我们通过使用光调毒/镍双催化剂体系报告具有各种胺偶联伴侣的(杂)芳基卤化物的C-N交叉偶联的可见光介导的流程方法。 与批次中的方法相比,该流程过程使得更宽的基材范围,包括较少激活的(杂)芳基溴和电子缺陷(杂)芳基氯,并显着降低反应时间(10至100分钟)。 此外,通过合成四丙酸的反应进行扩大,易于实现,以始终如一的高产率为84%,递送C-N的交叉偶联产物,高达10mmol级。

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