CHINESE JOURNAL OF ENERGETIC MATERIALS
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2,4,6-三硝基-2,4,6-三氮杂环己酮的合成研究进展
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作者单位:

(1. 南京理工大学化工学院, 江苏 南京 210094; ;2. 中国药科大学药学院, 江苏 南京 210009)

作者简介:

马丛明(1988-),男,博士生,主要从事含能材料的合成与应用研究。e-mail: maming1306@126.com

通讯作者:

姚其正(1951-),男,教授,主要从事含能材料的合成与应用研究,氮杂环药物研究。e-mail: qz_yao@yahoo.com.cn

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Progresss in Synthesis of 2,4,6-Trinitro-2,4,6-triazacyclohexanone
Author:
Affiliation:

(1. School of Chemical Engineering, Nanjing University of Science & Technology, Nanjing 210094, China; ;2. School of Pharmacy, China Pharmaceutical University, Nanjing 210009, China)

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    摘要:

    汇集、分析、评述了合成2, 4, 6-三硝基-2, 4, 6-三氮杂环己酮(Keto-RDX)的方法、途径、特点及原料和硝化体系。附22篇参考文献。认为:以脲和乌洛托品为原料合成Keto-RDX的直接法具有反应步骤少、成本低、产率高的优点和难分离提纯产物的缺点,而通过1, 3, 5-三嗪类中间体合成Keto-RDX的多步法具有反应步骤多,成本高的缺点和易分离提纯产物的优点。

    Abstract:

    The strategies, methods, paths, characters, starting materials and nitrating systems of synthesizing 2, 4, 6-trinitro-2, 4, 6-triazacyclohexanone(Keto-RDX) were summarized, analysized and reviewed with 22 references. Considering that direct method using urotropine and urea as starting materials has the advantages of less steps, lower cost and higher yield and the disadvantages of difficult separation and purification from a mixtures of Keto-RDX and RDX, while the multistep method of synthesizing Keto-RDX via 1, 3, 5-triazine intermediates has the disadvantages of more reaction steps and higher cost and the advantages of easier separation and purification.

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马丛明,刘祖亮,姚其正.2,4,6-三硝基-2,4,6-三氮杂环己酮的合成研究进展[J].含能材料, 2013, 21(1):126-130. DOI:10.3969/j. issn.1006-9941.2013.01.026.
MA Cong-ming, LIU Zu-liang, YAO Qi-zheng. Progresss in Synthesis of 2,4,6-Trinitro-2,4,6-triazacyclohexanone[J]. Chinese Journal of Energetic Materials, 2013, 21(1):126-130. DOI:10.3969/j. issn.1006-9941.2013.01.026.

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历史
  • 收稿日期: 2012-03-27
  • 最后修改日期: 2012-04-20
  • 录用日期: 2012-04-24
  • 在线发布日期: 2013-01-25
  • 出版日期: