Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | HCID 178526252 | HCID 178526252 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178507784 | HCID 178507784 | — |
| Product | HCID 178526712 | HCID 178526712 | 68% |
Reaction Steps
5-amino-2-hydroxypyridine-N-oxide was prepared as follows. One hundred grams of the 2-hydroxypyridine-N-oxide were dissolved in 500 mL of acetic acid with warming. The solution was cooled to approximately 10° C., and 65 mL of 70% nitric acid was added slowly to keep the temperature below 35° C. The mixture was stirred for an additional 30 min and the product was collected by filtration. After washing with acetic acid, and then water, the product was dried under vacuum at 70° C., to give 5-nitro-2-hydroxypyridine-N-oxide (95.9 g, 68% yield). 1HNMR data for this compound (DMSO) was as follows: δ 9.2 (d, 1H), 8.1 (dd, 1H), 6.6 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08858695B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-e4a82bc9995b4adb869d1b6499dd8fd1 |
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| Source note | uspto-grants-2014_10 |
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