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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483130Generated: October 25, 2026

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

https://huagongshe.com/reaction/483130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantWaterHCID 962—
ReactantChloroselenobenzeneHCID 21928—
Reactant1-Ethyl-2-oxocyclohexaneacetic Acid Methyl EsterHCID 12292028—
SolventTetrahydrofuranHCID 8028—
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 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 numberUS04578398
Source datasetuspto-grants-1986_03
ORD IDord-c4132d7101a34923b384dee437e76b1c
Source noteuspto-grants-1986_03