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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383839Generated: October 26, 2026

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

https://huagongshe.com/reaction/383839

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 stirret 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 numberUS08367676B2
Source datasetuspto-grants-2013_02
ORD IDord-6545365a0b0348e9849fae3bfbf04624
Source noteuspto-grants-2013_02