Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119183Generated: November 2, 2026

Hydrogen Peroxide → HCID 14010391, compound

https://huagongshe.com/reaction/2119183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
ReactantHCID 14010388HCID 14010388—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14010391HCID 14010391—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 15.0 g of 3-methallyl-4-pivaloyloxybenzophenone in 30 ml of THF was treated with 100 ml of 0.5M solution of 9-borabicyclo[3.3.1]nonane in THF at 0° C. The mixture was stirred at 25° C. for 3 h and at 50° C. for 1 h. To the cooled reaction mixture were added 30 ml of ethanol, 9.5 ml of 6N sodium hydroxide, and 18 ml of 30% hydrogen peroxide. After stirring at 25° C. for 2 h, the oxidation mixture was treated with solid potassium carbonate followed by a small amount of water. The organic layer was separated and dried over MgSO4. The crude product (22 g) was chromatographed on a silica gel column using toluene-ethyl acetate. 8.0 g of product was obtained as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04683241
Source datasetuspto-grants-1987_07
ORD IDord-9e1cd0aed3b240848bc4bcd9cf094971
Source noteuspto-grants-1987_07