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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976524Generated: October 29, 2026

p-Toluenesulfonic acid → 1(1-Naphthyl)-1-(tetrahydropyran-2yloxy)-2-[2(p-toluenesulfonyloxy)ethoxy]ethane

https://huagongshe.com/reaction/976524

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactant1(1Naphthyl)-2-[2-(p-toluenesulfonyloxy)ethoxy]ethanolHCID 54130037—
SolventDichloromethaneHCID 6344—
Product1(1-Naphthyl)-1-(tetrahydropyran-2yloxy)-2-[2(p-toluenesulfonyloxy)ethoxy]ethaneHCID 53718460—

Reaction Steps

0.82 g of pyridimium p-toluenesulfonate was added to a solution of 6.3 g of 1-(1-naphthyl)-2-[2-(p-toluenesulfonyloxy)ethoxy]ethanol and 2.97 ml of 3,4-dihydro-2H-pyran dissolved in 63 ml of methylene chloride at room temperature. The resulting mixture was stirred at the same temperature for 20 minutes and further at 35°-40° C. for 10 minutes. The reaction mixture was cooled, washed with water, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue thus obtained was purified by column chromatography (eluant: toluene/ethyl acetate=10/1) to obtain 7.53 g of colorless, oily 1(1-naphthyl)-1-(tetrahydropyran-2-yloxy)-2-[2-(p-toluenesulfonyloxy)ethoxy]ethane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05612381
Source datasetuspto-grants-1997_03
ORD IDord-b9e35ba9a10f4f62bedf6d4d40226c8e
Source noteuspto-grants-1997_03