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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633751Generated: October 29, 2026

4-Toluenesulfonyl chloride → 2-(Pyridin-3-yl)ethyl 4-methylbenzene-1-sulfonate

https://huagongshe.com/reaction/633751

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant3-PyridineethanolHCID 80515—
SolventDichloromethaneHCID 6344—
Product2-(Pyridin-3-yl)ethyl 4-methylbenzene-1-sulfonateHCID 8659736573.2%

Reaction Steps

6.62 mL (47.26 mmol) of triethylamine and 8.26 g (43.32 mmol) of 4-methylbenzenesulfonyl chloride are added at 0° C. to a solution of 5 g (39.38 mmol) of 2-pyrid-3-ylethanol in 300 mL of dichloromethane. After allowing the reaction medium to warm to room temperature and stirring overnight, it is washed with water and with saturated NaCl solution. The organic phase is dried over magnesium sulfate and evaporated to dryness. After purification by chromatography on silica gel (eluent: 4/6 heptane/EtOAc), 8 g of 2-pyrid-3-ylethyl toluene-4-sulfonate were obtained, corresponding to the following characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321790B2
Source datasetuspto-grants-2016_04
ORD IDord-5f628e2afad841388b4fdb6f637f4f0e
Source noteuspto-grants-2016_04