HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827322Generated: November 1, 2026
Hydrogen Peroxide → 1a,2a,3,6,6a,7a-Hexahydro-3,6-methanonaphtho[2,3-b]oxirene-2,7-dione
https://huagongshe.com/reaction/1827322
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1,4-Methanonaphthalene-5,8-dione, 1,4,4a,8a-tetrahydro- | HCID 79150 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1a,2a,3,6,6a,7a-Hexahydro-3,6-methanonaphtho[2,3-b]oxirene-2,7-dione | HCID 319927 | 98.35% |
Reaction Steps
A solution of tricyclo[6.2.1.02,7]undeca-4,9-diene-3,6-dione (14) (26.13 g, 150 mmol) in acetone (100 ml) was cooled to 0° C. on an ice-bath. To the solution was added saturated aqueous NaHCO3 (33 ml). To the mixture was added dropwise 34.5% aqueous hydrogen peroxide (142 ml) while keeping at 0° C. After the addition, the reaction mixture was stirred at 0° C. for 1 hr and then water (100 ml) was added. From the mixture solution, the product was extracted with diethyl ether (total 700 ml). The extract was washed with saturated aqueous NaCl and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure to afford as the residue 4,5-epoxy-tricyclo[6.2.1.02,7]undec-9-ene-3,6-dione (15) (28.06 g, 148 mmol, 98.35%., yield) in light yellowish white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07053224B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-88bbfd06a607445ebfa16dc3426f7819 |
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| Source note | uspto-grants-2006_05 |
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