化学学报 ›› 2025, Vol. 83 ›› Issue (4): 319-325.DOI: 10.6023/A25010008 上一篇    下一篇

研究通讯

光催化脱氢N-烷氧基酰胺类化合物的自偶联反应研究

刘冬霞, 卡迪尔亚•阿布都外力, 张迁, 李佳佳, 樊彦青*(), 阿布都热西提•阿布力克木*()   

  1. 新疆师范大学化学系 乌鲁木齐 830054
  • 投稿日期:2025-01-06 发布日期:2025-03-06
  • 基金资助:
    国家自然科学基金(地区基金)(22161046)

Self-Coupling Reactions of Photocatalyzed Dehydrogenated N-Alkoxyamide Compounds

Dongxia Liu, Abuduwaili Kadierya, Qian Zhang, Jiajia Li, Yanqing Fan(), Abudu Rexit Abulikemu()   

  1. Department of Chemistry, Xinjiang Normal University, Urumqi 830054, China
  • Received:2025-01-06 Published:2025-03-06
  • Contact: E-mail: fanyanqing@xjnu.edu.cn;aarexit@xjnu.edu.cn
  • Supported by:
    National Natural Science Foundation of China(22161046)

N—N键作为一种重要的化学键, 广泛存在于多种天然产物、材料和药物分子中, 并发挥着至关重要的作用. 本研究介绍了一种简便且高效的合成方法, 采用市售的伊红Y二钠盐作为光敏剂, 乙酸乙酯作为溶剂, 实现了在室温空气氛围及可见光照射下的N-烷氧基酰胺和二芳基胺类化合物的N—N自偶联反应. 此过程无需金属催化剂、配体或添加剂的参与, 以中等至良好的产率成功制备了肼类化合物. 该方法反应条件温和、操作简便、底物适用范围广泛, 且在太阳光条件下可以有效进行. 这一策略为肼类化合物的合成提供了一种简便、温和且经济的新途径.

关键词: 无氧化剂, 二芳基胺, 绿色溶剂, 肼类化合物

The N—N bond constitutes a fundamental structural motif in synthetic chemistry, ubiquitously present in organic compounds, natural products, and pharmaceutical agents. Beyond its structural significance, this bond demonstrates versatile functionalities in energy transfer systems, photoresponsive materials, and advanced dye technologies. Motivated by the critical importance of N—N bond formation, various synthetic methodologies have been explored. Among them, photocatalytic technology has stood out from numerous methods and become a highly regarded green organic synthesis means due to its mild conditions, environmental friendliness, and sustainable utilization. Based on this, this work reports the N—N self-coupling reaction of N-alkoxyamide and diarylamine compounds mediated by visible light. Employing commercially available Erythrosine Y disodium salt as the photosensitizer and ethyl acetate as the solvent, without metal catalysts, ligands and additives are required, a series of valuable functionalized hydrazines were provided at room temperature under air atmosphere with moderate to good yields. A total of 31 target compounds were synthesized, and the separation yield was up to 82%. Finally, the possible reaction mechanism was speculated through control experiments, hydrogen gas detection experiments, and relevant literature reports. This method not only features mild conditions and simple operation but also demonstrates good substrate universality, being applicable to various differently substituted benzene rings, aromatic heterocycles, and aliphatic amide substrates. Additionally, the target product can also be obtained with a separation yield of 49% under natural light conditions. It provides a simple, mild, and economical preparation approach for the synthesis of structurally complex hydrazine derivatives. The typical operational steps are as follows: In a 25 mL Schlenk tube, successively add N-alkoxyamide (0.2 mmol, 1 equiv.), Erythrosine Y disodium salt (2.5 mol%, 2.5% equiv.), and ethyl acetate (1 mL). Subject the reaction to irradiation at 10 W 413 nm LED for stirring and monitor the reaction progress using thin-layer chromatography (TLC). Once the starting materials are completely consumed, separate and purify the N—N self-coupling product using silica gel column chromatography.

Key words: no oxidant, diarylamine, green solvent, hydrazine compound