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4,4'-偶氮苯乙醚

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4,4'-偶氮苯乙醚
别名 4,4'-二乙氧基偶氮苯
识别
CAS号 588-52-3  checkY
性质
化学式 C16H18N2O2
摩尔质量 270.33 g·mol−1
外观 黄色固体[1]
熔点 156-158 °C[2]
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。

4,4'-偶氮苯乙醚是一种有机化合物,化学式为C16H18N2O2,它可由4,4'-氧化偶氮苯乙醚还原制得,[2]4-氨基苯乙醚的氧化偶联得到。[1]

反应

它在甲醇中可以被/联氨甲酸盐还原为1,2-二(4-乙氧基苯基)肼。[3]

它和氯化钯反应,可以得到配合物Pd22:C, N-L2)(μ-Cl)2(其中L为4,4'-二乙氧基偶氮苯-3-基)。[4]

参考文献

  1. ^ 1.0 1.1 Ádám Georgiádes; et al. Exploring New Parameter Spaces for the Oxidative Homocoupling of Aniline Derivatives: Sustainable Synthesis of Azobenzenes in a Flow System. ACS Sustainable Chem. Eng. 2015, 3, 12, 3388–3397. doi:10.1021/acssuschemeng.5b01096.
  2. ^ 2.0 2.1 Nanjundaswamy, H. M.; Pasha, M. A. (2005). Facile, Product‐Selective Reduction of Azoxyarenes into Azoarenes or Hydrazoarenes by Aluminium/Hydrazine Hydrate. Synthetic Communications, 35(16), 2163–2168. doi:10.1080/00397910500182275
  3. ^ Prasad, H. S.; Gowda, Shankare; Abiraj, K.; Channe Gowda, D. (2003). Catalytic Transfer Hydrogenation of Azo Compounds to Hydrazo Compounds Using Inexpensive Commercial Zinc Dust and Hydrazinium Monoformate. , 33(4), 717–724. doi:10.1081/sim-120020334.
  4. ^ Amanpreet K. Sandhu; et al. Cyclopalladation of azobenzenes and their reactivity towards N-substituted imidazolidine-2-thiones and allied ligands: Synthesis, structures, spectroscopy and ESI-mass studies. Journal of Organometallic Chemistry, 2018. 861. 112-124. doi:10.1016/j.jorganchem.2018.02.037.