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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859078Generated: October 25, 2026

Hydrogen Peroxide → 3'-Phenylspiro[indene-2,2'-oxirane]-1,3-dione

https://huagongshe.com/reaction/1859078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant2-Benzylidene-1,3-indandioneHCID 237822—
SolventMethanolHCID 887—
Product3'-Phenylspiro[indene-2,2'-oxirane]-1,3-dioneHCID 3142214—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a suspension of 2-benzylidene-1,3-indandione (20 g) in methanol (200 ml) was added 30% hydrogen peroxide (19 ml). The suspension was cooled to 5° C. and 1 N sodium hydroxide (2.1 ml) was added dropwise at such a rate as to keep the temperature below 15 ° C. After completed addition, stirring was continued at room temperature for 30 minutes. The mixture was then poured into water (1.2 L). The resulting crystalline precipitate was collected by filtration, washed on the filter with water (3×100 ml) and dried under high vacuum at room temperature for 24 hours, affording 3-phenylspiro[oxirane-2,2'-indan]-1',3'-dione as a yellow solid (17 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06153645
Source datasetuspto-grants-2000_11
ORD IDord-f5e821a3172d4116a7e7d12c233b35ab
Source noteuspto-grants-2000_11