Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | HCID 178515414 | HCID 178515414 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178526970 | HCID 178526970 | 120.4% |
Reaction Steps
Tetrazolo[1,5-a]quinolin-5-ol (10 g, 54 mmole, Example 1) was suspended in acetic acid (200 mL) then warmed to 40° C. Nitric acid (4 mL of 16M, 59 mmole) was added to the reaction mixture. The reaction mixture was heated at 80° C. for 30 minutes then allowed to cool to ambient temperature. The resulting precipitate was isolated by filtration, rinsed with water then recrystallized from isopropanol/water to provide 8.1 g of 4-nitrotetrazolo[1,5-a]quinolin-5-ol hydrate as light yellow plates, m.p. 186.5-187° C. Analysis: Calculated for C9H5N5O3. H2O: %C, 43.38; %H, 2.83; %N, 28.10; Found: %C, 43.27; %H, 2.84; %N, 28.25.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06437131B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-7c6a34d8fbe849819f940a82a9d5ddf9 |
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| Source note | uspto-grants-2002_08 |
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