HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243794Generated: October 30, 2026
Phosphorus oxychloride → 2-Chloro-4-methyl-nicotinonitrile
https://huagongshe.com/reaction/243794
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | 4-Methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile | HCID 10606782 | — |
| Product | 2-Chloro-4-methyl-nicotinonitrile | HCID 12387736 | 316.2% |
Reaction Steps
14 g (104 mmol) of 3-cyano-4-methylpyridone was slowly added to a mixture of 6.52 g (31.3 mmol) of phosphorus pentachloride and 30 ml (48 g, 313 mmol) of phosphorus oxychloride, followed by stirring at room temperature for 70 minutes and then under reflux with heating for 2 hours. After the reaction mixture was left to stand to cool, it was poured into ice water (400 ml) so that the surplus reagent was decomposed, followed by extraction with 100 ml of dichloromethane three times. The dichloromethane solution was washed with 100 ml of a saturated sodium chloride solution and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure to obtain 15.1 g of crude crystals of 2-chloro-3-cyano-4-methylpyridine. 1H-NMR (400 MHz, DMSO-d6): δ (ppm) 2.86 (s, 3H), 7.89 (d, J=5.6 Hz, 1H) 8.86 (d, J=5.6 Hz, 1H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653277B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-3fb6b493502b4d1995dcd675f1d1f69f |
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| Source note | uspto-grants-2014_02 |
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