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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742607Generated: October 29, 2026

4-Toluenesulfonyl chloride → (5-Ethyl-2-pyridyl)ethane p-toluenesulfonate

https://huagongshe.com/reaction/742607

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium HydroxideHCID 14798—
Reactant(5-Ethyl-2-pyridyl)ethanolHCID 19426344—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(5-Ethyl-2-pyridyl)ethane p-toluenesulfonateHCID 1942634893.2%

Reaction Steps

7.1 g of sodium hydroxide was dissolved in 33 ml of water, and 7.6 g of (5-ethyl-2-pyridyl)ethanol was dissolved in 33 ml of tetrahydrofuran. Both solutions were mixed and cooled. To the resultant solution was added dropwise gradually at 0° C. a solution of 11.7 g of p-toluenesulfonyl chloride in 51 ml of tetrahydrofuran, followed by stirring for 2 hours at the same temperature. To the reaction mixture was added ice water. The mixture was extracted twice with 100 ml each of methylene chloride. The extracted organic layers are combined. The resultant organic layer was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, whereby 14.4 g of (5-ethyl-2-pyridyl)ethane p-toluenesulfonate was obtained as a pale yellow oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05554758
Source datasetuspto-grants-1996_09
ORD IDord-e41048f6d0ef4cb9afce8798ae72002a
Source noteuspto-grants-1996_09