Nitrolysis of 3,5,9,11-Tetraacetyl-14-oxo-1,3,5,7,9,11-hexaazapentacyclo[5.5.3.0~(2,6).0~(4,10).0~(8,12)]pentadecane

Chinese Journal of Energetic Materials(2009)

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Abstract
In order to develop a new energetic materials,nitrolysis of 3,5,9,11-tetraacetyl-14-oxo-1,3,5,7,9,11-hexaazapentacyclo[5.5.3.02,6.04,10.08,12]pentadecane (Ⅰ) was studied in detail. Ⅰ was nitrolyzed selectively to 4-nitratomethyl-2,6,8,12-tetraacetyl-10-nitro-2,4,6,8,10,12-hexaazaisowurtzitane(Ⅱ) with HNO3/Ac2O. While with mixture of nitric and sulfuric acids as nitration reagent,at 80 ℃ directly or at 15 ℃ 2 h firstly then 80 ℃ Ⅰ was nitrolyzed to CL-20 or 4-nitratomethyl-2,6,8,10,12-pentanitrohezaazaisowurtzitane (Ⅲ) respectively. Ⅱcan also be nitrated to Ⅲ. The structures of two new hexaazaisowurtzitane derivatives(Ⅱand Ⅲ) were confirmed by MS,IR,1H NMR and 13C NMR.
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Heterocyclic Compounds
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