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METHOD OF SYNTHESIS OF 1,5-DINITRO-3,7-ENDO-METHYLENE-1,3,5,7- TETRAZACYCLOOCTANE

机译:1,5-二硝基-3,7-内-亚甲基-1,3,5,7-四环辛烷的合成方法

摘要

FIELD: organic chemistry, chemical technology. SUBSTANCE: invention relates to method of synthesis of cyclic nitroamines. Invention describes method of synthesis of 1,5-dinitro-endomethylene-1,3,5,7-tetrazacyclooctane. Method involves interaction of urea derivatives with methylolating agent, their decarboxylation followed by neutralization with aqueous ammonia and isolation of the end substance. Urea is used as the parent substance for synthesis of its derivatives and urea is treated with a mixture of sulfuric and nitric acids taken in the mass ratio = 1:(5- 10) at temperature 20 C - 20 C followed by successive mixing the prepared reactive mass with water at temperature 20 C, not above, with methylolating agent at temperature 0=60 C and ammonia at temperature 0-25 C. Formaldehyde or urotropin is used as a methylolating agent. Invention provides synthesis of the end substance based on available raw. EFFECT: improved method of synthesis, increased yield. 3 tbl
机译:领域:有机化学,化学技术。发明领域本发明涉及环状硝基胺的合成方法。本发明描述了合成1,5-二硝基-内亚甲基-1,3,5,7-四氮杂环辛烷的方法。方法涉及尿素衍生物与羟甲基化剂的相互作用,使其脱羧,然后用氨水中和并分离最终物质。尿素用作其衍生物合成的母体物质,尿素用质量比= 1:(5- 10)的硫酸和硝酸的混合物在20 C-20 C的温度下处理,然后连续混合制备的尿素。在20°C(不高于20°C)的温度下与水发生反应,在0 = 60°C的温度下与羟甲基化剂反应,在0-25°C的温度下与氨反应。甲醛或尿养蛋白用作羟甲基化剂。本发明提供了基于可用原料的最终物质的合成。效果:改进了合成方法,提高了收率。 3汤匙

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