Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762238Generated: October 31, 2026

Hydrogen Peroxide → 8-Oxabicyclo[5.1.0]octan-2-one

https://huagongshe.com/reaction/1762238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant2-Cyclohepten-1-oneHCID 70723—
SolventDiethyl EtherHCID 3283—
Product8-Oxabicyclo[5.1.0]octan-2-oneHCID 1561973380%

Reaction Steps

To a 0° C. solution of 50.0 g. (0.454 mmole) of cyclohept-2-en-1-one in 800 ml. of methanol was added 85 ml. of 30% hydrogen peroxide (0.75 mole) followed by the dropwise addition of 15 ml. of 6N sodium hydroxide (0.09 mole). The reaction was stirred for one hour and then added to 400 ml. ether-500 ml. petroleum ether. The ether extract was removed and the aqueous methanol phase extracted with four 500 ml. portions of petroleum ether and three 300 ml. portions of dichloromethane. The combined organic extracts were washed with three 800 ml. portions of saturated oodium chloride, dried over magnesium sulfate and evaporated under reduced pressure to an oil (53 g.). The crude oil was purified via vacuum distillation to yield 45.9 g. (80%) of the title compound as an oil. Caution: several forceful detonations have occurred during distillation of the crude product. (In general, however, the crude product is pure enough for further synthetic manipulations and distillation can be avoided.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04831059
Source datasetuspto-grants-1989_05
ORD IDord-f622ab2558cf4b77889f9df37480af41
Source noteuspto-grants-1989_05