7-(2,4,6-Trinitrophenyl)difurazano-furoxano-azepine compound
A technology of trinitrophenyl and furazan oxide is applied in the directions of nitrated acyclic/alicyclic/heterocyclic amine explosive compositions, organic chemistry, etc., and can solve the problems of low density, low thermal decomposition temperature, low detonation speed and the like
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[0019] At a temperature of 25°C, 7H-bisfurazolo[3,4-b:3',4'-f]furazolo[3",4"-d]azepine (0.47g , 2mmol) and 1-chloro-2,4,6-trinitrobenzene (0.495g, 2mmol) were added into anhydrous acetonitrile (5mL), stirred and dissolved. Slowly add NEt dropwise to it 3 (0.404g, 4mmol), continue to stir the reaction for 4h. After the reaction was completed, the solvent was evaporated to dryness, and the resulting crude product was rinsed with absolute ethanol to obtain brown powder 7-(2,4,6-trinitrophenyl)bisfurazanofurazanazepine 0.70g, yield 78.5%, purity 98.6%.
[0020] Structure Identification:
[0021] Infrared Spectrum: IR(KBr,cm -1 )ν: 3091, 1653, 1617, 1544, 1474, 1339, 1155, 1089, 996, 975, 920, 707;
[0022] NMR spectrum:
[0023] 1 H NMR (acetone-d 6 ,500MHz,ppm),δ:9.50(s,2H,C 6 h 2 );
[0024] 13 C NMR (acetone-d 6 ,125MHz,ppm),δ:153.62,153.07,150.42,148.53,144.17,137.70,135.53,128.96,127.18,105.51;
[0025] Elemental Analysis: Structural Formula C 12 h 2 N 10 o ...
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