HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642864Generated: October 27, 2026
Nitric Acid → 2-Amino-6-methyl-3-nitropyridine
https://huagongshe.com/reaction/642864
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Amino-6-methylpyridine | HCID 15765 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 2-Amino-6-methyl-3-nitropyridine | HCID 226028 | 19% |
Reaction Steps
6-Amino picoline (5.0 g, 46 mmol) was cautiously suspended in H2SO4 (25 ml) and cooled in an ice bath. Fuming nitric acid (5 ml) was added slowly, and care was taken to keep the temperature of the reaction as low as possible. The reaction mixture was allowed to stir 3 h after the addition of the nitric acid was complete. The mixture was added to sodium carbonate (65 g), suspended in about ice water (500 ml). Once the neutralization was complete, the aqueous mixture was extracted four times with ethyl acetate. The combined ethyl acetate washings were washed with brine, dried using MgSO4, and concentrated under vacuum to yield the title product (1.3 g, 19%) as a red oil. 1H NMR (DMSO-d6): δ=8.27 (d, 1H, J=8.5 Hz), 7.88 (bs, 2H), 6.63 (1H, d, J=8.5), 2.39 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696210B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-66fb8469d6ec44f885c091c3febe586a |
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| Source note | uspto-grants-2010_04 |
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