1,4‑Dihydroxy‑3,6‑Dinitropyrazolo[4,3‑c]pyrazole compounds
A technology of dinitropyrazole and compound, which is applied in the directions of nitrated acyclic/alicyclic/heterocyclic amine explosive composition, organic chemistry, etc., can solve the problems of low energy and low compound density, etc.
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[0020] (1) Synthesis of 3,6-dinitropyrazolo[4,3-c]pyrazole bis-ammonium salt
[0021] Under stirring, sequentially add 1.87g (9.44mmol) 3,6-dinitropyrazolo[4,3-c]pyrazole, 45.0mL methanol, and 8.0mL distilled water into the flask, and dropwise add 2.5mL 25%~ After the addition of 28% (mass) ammonia solution, the temperature was raised to 50°C for 6 hours, filtered, washed, and dried to obtain 3,6-dinitropyrazol[4,3-c]pyrazole bis-ammonium salt 1.90 g, the yield is 86.7%.
[0022] Structure Identification:
[0023] Infrared Spectrum: IR(KBr,cm -1 ), υ: 3141, 3.68 (-NH 4 + ), 1563, 1403, 1377 (-NO 2 ), 1292, 1175, 1042 (pyrazolopyrazole ring skeleton)
[0024] NMR spectrum: 1 HNMR (DMSO-d 6 ,500MHz), δ: 7.213(s,8H,2NH 4 + ); 13 CNMR (DMSO-d 6 ,125MHz), δ: 138.74,140.27
[0025] Elemental analysis: Molecular formula C 4 h 8 N 8 o 4
[0026] Theoretical value: C 20.69, H 3.47, N 48.27
[0027] Found values: C 20.77, H 3.42, N 48.32
[0028] The above structural...
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