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Acylation of 3,4-Diaminofurazan

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Journal of Beijing Institute of Technology 2013年第4期22卷 550-556页

作者：吴敏杰陈树森熊书玲金韶华李丽洁 School of Material Science and Engineering Beijing Institute of Technology

An acylation method of 3,4-diaminofurazan was developed. Under the catalysts of p-Tolu- enesulfonic acid, 3-amino-4-formylaminofurazan, 3-amino-4-acetylaminofurazan, 3-amino-4-propio- nylaminofurazan, 3-amino-4-butylramino-furazan and 3-amino-4-benzoylaminofurazan were synthe- sized by acylation of 3,4-diaminofurazan with formic acid, acetic acid, propionic acid, butyric acid and benzoic acid respectively. Also, 3,4-diacetylaminofurazan and 3,4-dipropionylaminofurazan were synthesized by acylation of 3,4-diaminofurazan with acetic anhydride and propionic anhydride re- spectively. Compared with the traditional method which uses acyl halogen as reagent, our method reduced the reaction time and increased the yield and purify. The 3-amino-4-acylaminofurazan could be hydrolyzed to 3,4-diaminofurazan in ethanol with acid catalyst.

关键词： furazan acylation 3-amino-4-acylaminofurazan 3,4-diacylaminofurazan

Synthesis of Two furazano Azides

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Journal of Beijing Institute of Technology 2001年第3期10卷 322-325页

作者：李战雄欧育湘陈博仁北京理工大学化工与材料学院北京100081

bis(azidomethyl) 3,3′ bis(1,2,4 oxadiazole)(Ⅰ) and bis(azidoacetamino) oxazofurazan(Ⅱ) were synthesized. The structures of these two compounds have been identified by IR, 1H NMR, MS and elemental analysis. Azido groups were introduced into furazan derivatives and energetic materials of high nitrogen content and high enthalpy of formation can be obtained. The densities of compound Ⅰ and Ⅱ are relatively high. Compound Ⅰ is an azide of lower melting point, it is hopeful to be applied as energetic plastic additives.

关键词： synthesis azide furazan

Recent advances on the nitrogen-rich 1,2,4-oxadiazole-azoles-based energetic materials

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Defence Technology（防务技术） 2022年第3期18卷 344-367页

作者： Wen-Li Cao Qamar-un-Nisa Tariq Zhi-Min Li Jun-Qing Yang Jian-Guo Zhang State Key Laboratory of Explosion Science and Technology Beijing Institute of TechnologyBeijing100081 PR China CAS Key Laboratory of Energy Regulation Materials Shanghai200032China

This review covers recent advances in the synthesis and energetic performance of nitrogen-rich 1,2,4-oxadiazole-azoles-based energetic *** materials comprise of 1,2,4-oxadiazole subunit as a key structural motif linked to different nitrogen-rich or nitrogen-oxygen azoles:tetrazole,furazan,furoxan,1,3,4-oxadiazole,pyrazole,and *** attention is devoted to the introduction of various energetic groups including nitro,nitramino,azo,azoxy,dinitromethyl,trinitroethyl moieties,and their *** physicochemical and available performance parameters including density,decomposition temperature,heat of formation,detonation pressure,detonation velocity,impact sensitivity,and friction sensitivity of typical energetic compounds are also provided and ***,it was obtained that several screened compounds exhibit superior detonation properties and outstanding insensitivities,which can be classified as a new family of high-performance energetic ***,1,2,4-oxadiazole-azoles-based energetic materials still have many thorough works to further exploited and studied,expecting to get very promising insensitive high explosives for practical application and industrialization.

关键词： 1,2,4-Oxadiazole-azoles Triazole Tetrazole furazan Energetic materials Furoxan