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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448632Generated: October 25, 2026

Hydrogen Peroxide → 2,3-Epoxy-4-(2-tetrahydropyranyloxy)cyclopentan-1-one

https://huagongshe.com/reaction/1448632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
Reactant4-(Tetrahydro-pyran-2-yloxy)-cyclopent-2-enoneHCID 12838010—
Reactant4-t-Butyldimethylsiloxy-2-n-octylthiocyclopent-2-en-1-oneHCID 20380374—
SolventMethanolHCID 887—
Product2,3-Epoxy-4-(2-tetrahydropyranyloxy)cyclopentan-1-oneHCID 2038034784%

Reaction Steps

One gram of 4-(2-tetrahydropyranyloxy)cyclopent-2-en-1-one was dissolved in 20 ml of methanol, and 10 ml of 30% hydrogen peroxide was added at room temperature. Then, with ice cooling, 3 ml of a 2 N aqueous solution of sodium hydroxide was added slowly. The mixture was stirred at room temperature for 1.5 hours. The reaction mixture was post-treated in the same way as in Example 1, (1). The resulting crude product was chromatographed on a thin layer plate with cyclohexane/ethyl acetate (=7/3) to afford 730 mg of 2,3-epoxy-4-(2-tetrahydropyranyloxy)cyclopentan-1-one in a yield of 84%. The product had the following spectral data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04180672
Source datasetuspto-grants-1979_12
ORD IDord-5f425e3822f0430cbb3da60d10d1f887
Source noteuspto-grants-1979_12