Chin. J. Org. Chem. ›› 2009, Vol. 29 ›› Issue (05): 798-801. Previous Articles     Next Articles

Reports

氨基呋咱氧化为氨基硝基呋咱的合成研究

李洪珍*; 李金山 ; 黄 明 ; 周小清   

  1. (中国工程物理研究院化工材料研究所 绵阳 621900)
  • 收稿日期:2008-07-19 修回日期:2008-10-03 发布日期:2009-05-20
  • 通讯作者: 李洪珍

Synthesis of Aminonitrofurazan by Oxidizing Aminofurazan

Li, Hongzhen* ; Li, Jinshan ; Huang, Ming ; Zhou, Xiaoqing
  

  1. (Institute of Chemical Materials, China Academy of Engineering Physics, Mianyang 621900)
  • Received:2008-07-19 Revised:2008-10-03 Published:2009-05-20
  • Contact: Li, Hongzhen

The new general synthetic method has been developed for the convenient preparation of aminonitrofurazans. The synthesis of 3-amino-4-nitrofurazan (ANF), 3-amino-3’-nitro-4,4’-azoxyfurazan (ANAF) and 3-amino-3’-nitro-4,4’-azofurazan (ANAzF) were achieved by oxidizing 3,4-diaminofurazan (DAF), 3,3’-diamino-4,4’-azoxyfurazan (DAAF) and 3,3’-diamino-4,4’-azofurazan (DAAzF) respectively, with the oxidizing mixtures of hydrogen peroxide, sodium tungstate or ammonium persulfate and methanesulfonic acid [H2O2/CH3SO3H/Na2WO4 or (NH4)2S2O8] with reduced acidity to give above 65% yield of ANF and ANAF, and 15% yield of ANAzF. The experiments showed that the mixture of H2O2 and Na2WO4 or (NH4)2S2O8) in CH3SO3H media is a new kind of efficient oxidant for the synthesis of one or more furazan rings with amino and nitro groups.

Key words: synthesis, aminofurazan, aminonitrofurazan, energetic material