HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466564Generated: October 31, 2026
Nitric Acid → 5-Bromo-2-methyl-4-nitropyridine 1-oxide
https://huagongshe.com/reaction/1466564
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 5-Bromo-2-methylpyridin-1-ium-1-olate | HCID 817164 | — |
| Product | 5-Bromo-2-methyl-4-nitropyridine 1-oxide | HCID 12332908 | 90.3% |
Reaction Steps
5-bromo-2-methylpyridine 1-oxide (2.269 g, 12.07 mmol, 1 eq) was dissolved in sulfuric acid (4 mL, 80 mmol, 6 eq) and cooled at 0° C. Fuming nitric acid (3 mL, 60 mmol, 5 eq) was added dropwise. After addition of the nitric acid was complete, the reaction mixture was first warmed to room temperature and then heated to 90° C. After 2 hours the reaction was cooled in an ice bath and slowly adjusted to pH 10 with 2 M aqueous sodium carbonate. This solution was extracted twice with dichloromethane. The combined organic extracts were dried over magnesium sulfate and concentrated to yield 2.54 g (90%) of 5-bromo-2-methyl-4-nitropyridine 1-oxide. LMCS (ESI) m+H=233.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999998B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-d3f9b9e53c3447848a92c5aaf2e64872 |
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| Source note | uspto-grants-2015_04 |
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