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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888002Generated: October 25, 2026

Triethylamine → 2,6-Dichloro-3-methylpyridine

https://huagongshe.com/reaction/1888002

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 81708821%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501770B2
Source datasetuspto-grants-2013_08
ORD IDord-f4e8c51547454b33b4838295e8fb605d
Source noteuspto-grants-2013_08