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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295984Generated: October 30, 2026

Triethylamine → 5-(Chloromethyl)-2-methylpyridine

https://huagongshe.com/reaction/1295984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant(6-Methylpyridin-3-yl)methanolHCID 11228788—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product5-(Chloromethyl)-2-methylpyridineHCID 1221433837.5%

Reaction Steps

Triethylamine (96 ml, 0.69 mol) was added to a solution of (6-methyl-3-pyridyl)methanol (28.4 g, 0.23 mol) in methylene chloride (230 ml) while cooling on ice. Mesyl chloride (26.8 ml, 0.35 mol) was then slowly added dropwise over a period of 20 minutes at the same temperature and the mixture was stirred for 10 hours while gradually raising the temperature to room temperature. After confirming completion of the reaction by thin layer chromatography, the mixture was diluted with ethyl acetate and poured into saturated aqueous NaHCO3. After separating the aqueous layer, extraction was performed with ethyl acetate, and the collected organic layer was washed with saturated aqueous NaCl and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to yield the title compound (12.2 g). This was used without further purification for the following reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244730B2
Source datasetuspto-grants-2007_07
ORD IDord-e3b3468ae3294f408a8e1e793ac922ce
Source noteuspto-grants-2007_07