HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724014Generated: October 27, 2026
Phosphorus oxychloride → 2-Chloro-4,6-dimethyl-3-nitropyridine
https://huagongshe.com/reaction/724014
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 4,6-Dimethyl-3-nitropyridin-2(1H)-one | HCID 535972 | — |
| Product | 2-Chloro-4,6-dimethyl-3-nitropyridine | HCID 21875578 | 180.4% |
Reaction Steps
A mixture of 4,6-dimethyl-3-nitro-2(1H)-pyridinone (step 1, 10.0 g, 29.7 mmol) in phosphorus oxychloride (35 mL, 187.3 mmol) was stirred at 95° C. for 3 h, then cooled to 45° C. The excess amount of phosphorus oxychloride was removed by distillation under reduced pressure at 45° C. The residue was cooled to room temperature, and diluted with dichloromethane (75 mL). The resulting solution was cooled to 0° C., and 2N hydrochloric acid (50 mL) was added dropwise into the solution. The organic layer was separated, and washed with 2N hydrochloric acid (4×25 mL), 2N aqueous NaOH (2×50 mL) and brine (50 mL). The organic phase was dried (MgSO4) and concentrated under reduced pressure to give 10.0 g (90%) of the title compound as white solids: 1H-NMR (CDCl3) δ 7.07 (1H, s), 2.56 (3H, s), 2.35 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07141580B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-afa9507ce2fe4c4890a4133f403917ce |
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| Source note | uspto-grants-2006_11 |
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