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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantWaterHCID 962—
Reactant1,4-Methanonaphthalene-5,8-dione, 1,4,4a,8a-tetrahydro-HCID 79150—
ReactantSodium BicarbonateHCID 516892—
SolventAcetoneHCID 180—
Product1a,2a,3,6,6a,7a-Hexahydro-3,6-methanonaphtho[2,3-b]oxirene-2,7-dioneHCID 31992798.35%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053224B2
Source datasetuspto-grants-2006_05
ORD IDord-88bbfd06a607445ebfa16dc3426f7819
Source noteuspto-grants-2006_05