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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535667Generated: October 25, 2026

4-Toluenesulfonyl chloride → 2-(6-Methoxypyridin-2-yl)ethyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/535667

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant2-(6-Methoxypyridin-2-yl)ethan-1-olHCID 15319871—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product2-(6-Methoxypyridin-2-yl)ethyl 4-methylbenzenesulfonateHCID 59636776—

Reaction Steps

A solution of 2-(6-methoxypyridin-2-yl)ethanol (0.23 g, 1.50 mmol), 4-dimethylaminopyridine (0.028 g, 0.23 mmol), triethylamine (0.63 mL, 4.50 mmol) and p-toluenesulfonyl chloride (0.34 g, 1.80 mmol) in dry dichloromethane (5 mL) was stirred at rt over night. The solvent was removed in vacuo. Ethyl acetate and water were added. The organic phase was separated and the aqueous phase was extracted with ethyl acetate. The combined organic phases were dried (Na2SO4) and concentrated. The product was purified by flash chromatography (SiO2; heptane/EtOAc, gradient 0-100%). Yield: 0.18 g (38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859534B2
Source datasetuspto-grants-2014_10
ORD IDord-70334fdf56194307bd8210e70a762595
Source noteuspto-grants-2014_10