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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329519Generated: October 31, 2026

Diethyl Ether → 2-[7-(Tetrahydropyran-2-yloxy)heptyloxymethyl]tetrahydropyran-3-one

https://huagongshe.com/reaction/329519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium AcetateHCID 517045—
Reactanttrans-2-[7-(Tetrahydropyran-2-yloxy)heptyloxymethyl]tetrahydropyran-3-olHCID 18637142—
ReactantHCID 178526118HCID 178526118—
SolventDichloromethaneHCID 6344—
Product2-[7-(Tetrahydropyran-2-yloxy)heptyloxymethyl]tetrahydropyran-3-oneHCID 15097255—

Reaction Steps

A solution of 2.387 g of dl-trans-2-[7-(tetrahydropyran-2-yloxy)heptyloxymethyl]tetrahydropyran-3-ol (prepared as described in Preparation 54) in 10 ml of methylene chloride was added all at once to a mixture of 2.33 g of pyridine chlorochromate, 1.78 g of sodium acetate and 10 ml of methylene chloride. The mixture was then stirred at room temperature for 3 hours, after which it was mixed with 30 ml of diethyl ether, and the solution was passed through a chromatography column containing 50 g of silica gel. The column was then washed with diethyl ether and the eluate was combined with the washings and then concentrated by evaporation under reduced pressure. The oily residue (2.24 g) was subjected to column chromatography through 60 g of silica gel. 1.786 g of the title compound was obtained, as an oil, from those fractions eluted with mixtures of hexane and ethyl acetate ranging from 3:1 to 2:1 by volume.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04891363
Source datasetuspto-grants-1990_01
ORD IDord-f4a5ac5c066641efaece65823556e111
Source noteuspto-grants-1990_01