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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505385Generated: October 25, 2026

Triethylamine → 2,6-Dichloro-3-methylpyridine

https://huagongshe.com/reaction/505385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-Chloro-3-methyl-1-oxo-1lambda~5~-pyridineHCID 13431622—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2,6-Dichloro-3-methylpyridineHCID 81708834.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781452B2
Source datasetuspto-grants-2010_08
ORD IDord-11c8505cb0f04b76b84398dbdf22bb27
Source noteuspto-grants-2010_08