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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Benzylidene-1,3-indandione | HCID 237822 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3'-Phenylspiro[indene-2,2'-oxirane]-1,3-dione | HCID 3142214 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06153645 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-f5e821a3172d4116a7e7d12c233b35ab |
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| Source note | uspto-grants-2000_11 |
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