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首页> 外文期刊>Organic & biomolecular chemistry >Palladium-catalyzed ortho-acyloxylation of N-nitrosoanilines via direct sp~2 C-H bond activation
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Palladium-catalyzed ortho-acyloxylation of N-nitrosoanilines via direct sp~2 C-H bond activation

机译:通过直接的sp〜2 C-H键活化,钯催化N-亚硝基苯胺的邻位酰氧基化

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摘要

The palladium-catalyzed N-nitroso-directed ortho-acyloxylation of N-nitrosoanilines has been demonstrated via sp~2 C-H activation with a stoichiometric amount of Phl(OAc)_2 as the oxidant and Ac_2O/AcOH (1:1) or C_2H_5CO_2H as the reaction medium. This protocol can be applied to various N-nitrosoanilines with both electron-donating and electron-withdrawing groups. In addition, the products can be further transformed to 2-(methylamino)phenols expediently by a simple reduction method.
机译:已通过sp〜2 CH活化,化学计量的Phl(OAc)_2作为氧化剂和Ac_2O / AcOH(1:1)或C_2H_5CO_2H作为钯,证明了钯催化的N-亚硝基苯胺的N-亚硝基定向的邻酰氧基化反应。反应介质。该协议可以应用于带有给电子基团和吸电子基团的各种N-亚硝基苯胺。另外,可以通过简单的还原方法方便地将产物进一步转化为2-(甲基氨基)苯酚。

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  • 来源
    《Organic & biomolecular chemistry》 |2015年第25期|6958-6964|共7页
  • 作者单位

    Hefei National Laboratory for Physical Sciences at Microscale, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), and Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, P. R. China;

    Hefei National Laboratory for Physical Sciences at Microscale, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), and Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, P. R. China;

    Hefei National Laboratory for Physical Sciences at Microscale, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), and Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, P. R. China,State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou, Gansu 730000, P. R. China;

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