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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197049Generated: October 30, 2026

Hydrogen Peroxide → HCID 15728606, compound

https://huagongshe.com/reaction/1197049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 14837915HCID 14837915—
SolventMethanolHCID 887—
ProductHCID 15728606HCID 1572860653%
ProductHCID 15728607HCID 1572860734%

Reaction Steps

To a solution of 2.49 g of 4-trimethylsilyloxy-4-(4-phenoxybutyl)-2-cyclopentenone dissolved in 50 ml of methanol was added 3.9 ml of an aqueous 30% hydrogen peroxide under ice-cooling and stirring. An amount of 390 μl of 1N aqueous sodium hydroxide was added, and the mixture was stirred for 2 hours. Then saturated aqueous ammonium chloride was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate. After filtration and concentration, the concentrate was subjected to silica gel column chromatography to give 892 mg (yield 34%) of 2,3-epoxy-4-trimethylsilyloxy-4-(4-phenoxybutyl)cyclopentanone and 1.38 g (yield 53%) of 2,3-epoxy-4-hydroxy-4-(4-phenoxybutyl)cyclopentanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116869
Source datasetuspto-grants-1992_05
ORD IDord-d64c022250344d96924afb133a07ccf8
Source noteuspto-grants-1992_05