Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247645Generated: October 26, 2026

Hydrogen Peroxide → 6-Carbomethoxymethyl-6-ethyl-2-cyclohexen-1-one

https://huagongshe.com/reaction/247645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
Reactant1-Ethyl-2-oxocyclohexaneacetic Acid Methyl EsterHCID 12292028—
SolventEthyl AcetateHCID 8857—
Product6-Carbomethoxymethyl-6-ethyl-2-cyclohexen-1-oneHCID 1364924155.3%

Reaction Steps

The ketone, 2-carbomethoxymethyl-2-ethylcyclohexanone (IX) (141 mmol, 28 g) was stirred in 1.25 L of ethyl acetate (dried over 3A molecular sieves) and treated with 169 mmol (32.5 g) of PhSeCL. The reaction was stirred under nitrogen for 4 hours then treated with 250 mL of water. The mixture was shaken vigorously in a separatory funnel and the organic phase was returned to the reaction flask. Tetrahydrofuran (550 mL) was then added followed by 35 mL of 30% H2O2 (aq.) added dropwise. The reaction mixture was stirred for one hour then washed with 500 mL of water and 500 mL of saturated Na2CO3 (aq.). The product was then dried over MgSO4 and concentrated in vacuo. Flash chromatography (4 inches diameter column, 20% ethyl acetate in petroleum ether eluent, 51/2 inches of silica gel) afforded 15.3 g (78.0 mmol, 55%) of the product as a pale yellow oil. Rf =0.9 in 15% ethyl acetate/petroleum ether on TLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04709048
Source datasetuspto-grants-1987_11
ORD IDord-e2b80fb30e254a9e90a1ad55bc671bde
Source noteuspto-grants-1987_11