4,4'-偶氮苯乙醚

化合物

4,4'-偶氮苯乙醚是一種有機化合物,化學式為C16H18N2O2,它可由4,4'-氧化偶氮苯乙醚還原製得,[2]4-氨基苯乙醚的氧化偶聯得到。[1]

4,4'-偶氮苯乙醚
別名 4,4'-二乙氧基偶氮苯
識別
CAS號 588-52-3  checkY
性質
化學式 C16H18N2O2
摩爾質量 270.33 g·mol−1
外觀 黃色固體[1]
熔點 156-158 °C[2]
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。

反應

它在甲醇中可以被/聯氨甲酸鹽還原為1,2-二(4-乙氧基苯基)肼。[3]

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

參考文獻

  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.