HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888002Generated: October 25, 2026
Triethylamine → 2,6-Dichloro-3-methylpyridine
https://huagongshe.com/reaction/1888002
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2-Chloro-3-methyl-1-oxo-1lambda~5~-pyridine | HCID 13431622 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,6-Dichloro-3-methylpyridine | HCID 817088 | 21% |
Reaction Steps
A solution of 2-chloro-3-methylpyridine 1-oxide (11.37 g, 79.2 mmol) and triethylamine (13.1 ml, 94.0 mmol) in dichloromethane (90 mL) at 0° C. was slowly treated with a solution of phosphorus oxychloride (8.8 ml, 96.1 mmol) in dichloromethane (35 mL) and stirred for a further 2 hours then heated to reflux for 1 hour. Water (40 mL) was added to the reaction mixture then it was basified with 2N sodium hydroxide (150 mL). The mixture was extracted with dichloromethane (3×100 mL) and the combined extracts were dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The product was purified by flash column chromatography on silica gel (160 g) 100% dichloromethane to afford 2,6-dichloro-3-methylpyridine as a white solid (2.64 g, 21%). 400 M Hz 1H NMR (DMSO-d6) δ: 7.86 (d, J=8.4 Hz, 1H), 7.47 (d, J=8.0 Hz, 1H), 2.30 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501770B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-f4e8c51547454b33b4838295e8fb605d |
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| Source note | uspto-grants-2013_08 |
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