HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505385Generated: October 25, 2026
Triethylamine → 2,6-Dichloro-3-methylpyridine
https://huagongshe.com/reaction/505385
Participants
| Role | Name | HCID | Charge |
|---|
| 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 | 34.2% |
Reaction Steps
2-Chloro-3-methylpyridine 1-oxide (9.00 g, 62.7 mmol) and triethylamine (10.4 ml, 75.2 mmol) were dissolved in dichloromethane (70 ml), and a solution of phosphorus oxychloride (7 ml, 75.3 mmol) in dichloromethane (40 ml) was added dropwise at 0° C. After stirring for 3 hours while elevating reaction temperature to room temperature, the reaction mixture was stirred under reflux for 1 hour. After the reaction was completed, water (30 ml) was added and the reaction mixture was neutralized with a sodium hydroxide solution, and after extracted with dichloromethane (70 ml), dried over magnesium sulfate. The solvent was evaporated and purified by silica gel column chromatography (eluting solvent: ethyl acetate/n-hexane=3/100), thereby yielding the title compound (3.47 g) as a white solid 10:3 mixture with 2,4-dichloro-3-methylpyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07781452B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-11c8505cb0f04b76b84398dbdf22bb27 |
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| Source note | uspto-grants-2010_08 |
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