New Method for Synthesis of 7-Amino-4,6-Dinitro-Benzofuroxan
An insensitive explosive, 7-amino-4,6-dinitro- benzofuroxan, was synthesized via condensation, nitration, azidation-denitrogenation and hydrolysis from the starting materials of m-chloroaniline, with the yields of 95.4%, 82.0%, 84.0% and 85.5% respectively. In the first reaction, amino group was protected with chloroacetylation. The conditions of the synthesis are mild and safe. The pyrolysis of denitrogenation after azidation in one pot took place at 80C, and all the other reactions proceeded at room temperature. The title compound was analyseded by means of H NMR, IR, MS, and elemental analysis.
benzofuroxans 7-amino-4,6- dinitrc-benzoruroxan insensitive explosive synthesis
WANG Jianlong LU Lianying SUN Yaoran MU Wei OU Yuxiang
School of Chemical Engineering and Environment, North University of China, Taiyuan 030051, Shanxi, C Chemistry Department, Shijiazhuang University, Shijiazhuang 050035, Hebei, China School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081, China
国际会议
西安
英文
604-605
2007-10-23(万方平台首次上网日期,不代表论文的发表时间)