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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257555Generated: November 1, 2026

3,4-dihydro-2H-pyran → 1(1-Naphthyl)-1-(tetrahydropyran-2yloxy)-2-[2(p-toluenesulfonyloxy)ethoxy]ethane

https://huagongshe.com/reaction/2257555

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
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 pyridinium 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 numberUS05658904
Source datasetuspto-grants-1997_08
ORD IDord-96228a9dc2ba4c289280094ffd9a81cd
Source noteuspto-grants-1997_08