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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802375Generated: October 26, 2026

4-Toluenesulfonyl chloride → 2-(tetrahydro-2H-pyran-4-yl)ethyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/1802375

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant2-(Oxan-4-yl)ethan-1-olHCID 17750944—
SolventPyridineHCID 1049—
Product2-(tetrahydro-2H-pyran-4-yl)ethyl 4-methylbenzenesulfonateHCID 5926796453.5%

Reaction Steps

To a solution of 1.63 g (12.5 mmol) of 2-(tetrahydro-pyran-4-yl)-ethanol in pyridine (15 mL) are added 3.58 g (18.8 mmol) of p-toluenesulfonylchloride. The reaction is stirred at room temperature for 5 h. The reaction mixture is concentrated under reduced pressure. The residue is dissolved 2M aqueous HCl solution (20 mL) and extracted with ethyl acetate (3×50 mL). The combined organic extracts are dried over Na2SO4, filtered and the solvent is removed to give 1.9 g of toluene-4-sulfonic acid 2-(tetrahydro-pyran-4-yl)-ethyl ester as off-white crystalline solid. Yield: 53%; ES-MS: m/z 285 [M+H]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349871B2
Source datasetuspto-grants-2013_01
ORD IDord-174b9f7698d344bf87e6968aea5097ab
Source noteuspto-grants-2013_01