HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267617Generated: November 2, 2026
Hydrogen Peroxide → 1,2,5-Oxadiazol-3-amine, 4,4'-azoxybis-
https://huagongshe.com/reaction/1267617
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3,4-Diaminofurazan | HCID 537677 | — |
| Reactant | HCID 4778074 | HCID 4778074 | — |
| Product | 1,2,5-Oxadiazol-3-amine, 4,4'-azoxybis- | HCID 533871 | 88% |
Reaction Steps
This procedure was modeled from the original Russian preparation. To 30% hydrogen peroxide (100.0 g, 0.88 mol) in a 500 ml jacketed flask maintained at 18° C. was added 98% sulfuric acid (55.0 g, 0.56 mol) over 10 minutes with stirring. Then, 3,4-diaminofurazan (10.0 g, 0.10 mole) was added. The suspension was stirred for 24 hours in which time the soluble green nitroso-amino-furazan was converted to the insoluble orange DAAF. The product was filtered on a glass frit, washed with water and air dried to yield 9.29 g (88%) of crude material. For recrystallization the crude compound was dissolved in the minimum amount of room temperature DMSO (approximately 22 ml) and then water (45 ml) was added over 5 minutes with stirring. The pure DAAF was filtered, washed with water and air-dried. This material had the same properties as previously reported by the Russians. 1H NMR (deuteriomethylsulfoxide)δ 6.65 (s, 2H), 6.93 (s, 2H); 13C NMR (deuteriomethylsulfoxide) δ 148.3, 151.2, 152.6, 153.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06552201B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-083705a72ae64ed4b85e296fab1da6ba |
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| Source note | uspto-grants-2003_04 |
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