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A Multicomponent Electrosynthesis of 1,5-Disubstituted and 1-Aryl 1,2,4-Triazoles

机译:1,5-二取代和1-芳基1,2,4-三唑的多组分电气合成

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摘要

A novel electrochemical route has been developed for the synthesis of 1,5-disubstituted and 1-aryl 1,2,4-triazoles from aryl hydrazines, paraformaldehyde, NH4OAc, and alcohols. In this multi component reaction system, alcohols act as solvents as well as reactants and NH4OAc is used as the nitrogen source. With the assistance of reactive iodide radical or I-2 and NH3 electrogenerated in situ, this process could effectively avoid the use of strong oxidants and transition-metal catalysts and be smoothly carried out at room temperature to give a wide array of 1,2,4-triazole derivatives in good to high yields. Preliminary studies reveal that the reaction mechanism involves a radical process.
机译:已经开发了一种新型电化学途径,用于合成1,5-二取代的1-芳基1,2,4-三唑,来自芳基肼,多聚甲醛,NH 4 OC和醇。 在该多组分反应体系中,醇用作溶剂以及反应物,NH 4℃用作氮源。 通过反应性碘化物的辅助或I-2和NH 3原位电流,该方法可以有效地避免使用强氧化剂和过渡金属催化剂,并在室温下平滑地进行,以提供各种1,2次, 4-三唑衍生物良好的产量。 初步研究表明,反应机制涉及自由基过程。

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  • 来源
    《The Journal of Organic Chemistry》 |2018年第19期|共7页
  • 作者

    Yang Na; Yuan Gaoqing;

  • 作者单位

    South China Univ Technol Sch Chem &

    Chem Engn Key Lab Funct Mol Engn Guangdong Prov Guangzhou 510640 Guangdong Peoples R China;

    South China Univ Technol Sch Chem &

    Chem Engn Key Lab Funct Mol Engn Guangdong Prov Guangzhou 510640 Guangdong Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
  • 关键词

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