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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419853Generated: November 2, 2026

4-Toluenesulfonyl chloride → 2-(Chloromethyl)-4-methylpyridine

https://huagongshe.com/reaction/1419853

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantPotassium CarbonateHCID 11430—
Reactant2,4-Dimethylpyridine 1-oxideHCID 70733—
Solvent1,4-DioxaneHCID 31275—
Product2-(Chloromethyl)-4-methylpyridineHCID 12675261364.4%

Reaction Steps

2,4-Lutidine-1-oxide (10 g, 8.10 mmol) was dissolved in anhydrous dioxane (125 ml) under nitrogen atomsphere, and herein p-toluenesulfonyl chloride (31.5 g, 162 mmol) was added and refluxed for 5 hours. The solution was neutralized with the saturated aqueous solution of potassium carbonate and extracted twice with methylene chloride. The combined organic layers were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to get crude product. The residue was separated and purified by column-chromatography over silica gel to obtain 2-chloromethyl-4-methylpyridine (4.18 g, yield=36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05889027
Source datasetuspto-grants-1999_03
ORD IDord-89510358d4574b16ad92508c4a546108
Source noteuspto-grants-1999_03