HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485511Generated: November 1, 2026
2,6-Dichloro-3-nitropyridine → 6-Chloro-3-nitropyridine-2-carbonitrile
https://huagongshe.com/reaction/1485511
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dichloro-3-nitropyridine | HCID 85239 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 6-Chloro-3-nitropyridine-2-carbonitrile | HCID 13381705 | 44.5% |
Reaction Steps
To a solution of 2,6-dichloro-3-nitropyridine (6.00 g, 31.1 mmol) in NMP (23.0 mL) was added copper(I) cyanide (3.06 g, 34.2 mmol) at room temperature. After stirred for 40 min at 180° C., the reaction mixture was cooled to room temperature, and then poured into ice water. After stirring for 10 min, the mixture was extracted with EtOAc, washed with brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The residue was purified by column chromatography on SiO2 (Hex:EtOAc=10:1) to give 6-chloro-3-nitropicolinonitrile (2.54 g, 44%) as a yellow solid. 1H-NMR (CDCl3, Varian 400 MHz) δ 7.79 (1H, d, J=8.4 Hz), 8.58 (1H, d, J=8.4 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422298B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-4de656b40a284869bf188497b4d790c8 |
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| Source note | uspto-grants-2016_08 |
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