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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084460Generated: October 26, 2026

tert-Butyl hydroperoxide → 1-Methoxy-1-(1,1-dimethylethylperoxy)cyclohexane

https://huagongshe.com/reaction/1084460

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl hydroperoxideHCID 6410—
Reactant1,1-DimethoxycyclohexaneHCID 13616—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventDimethyl SulfoxideHCID 679—
Product1-Methoxy-1-(1,1-dimethylethylperoxy)cyclohexaneHCID 1457303564.4%

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixed solution consisting of 16.4 g of dimethyl sulfoxide and 1.2 g of p-toluenesulfonic acid was kept at 20° C., and another mixed solution consisting of 28.9 g of cyclohexanone-dimethylacetal and 18.5 g of 1,1-dimethylethyl hydroperoxide was dropwise added to the former mixed solution. The resulting solution has an acid concentration of 0.1 mol/kg of the solution. The solution was stirred at 20° C. for 3 hours to complete the reaction. Then, 20 ml of petroleum ether was added to the solution, and the resulting solution was washed with 10 ml of water, then with 50 ml of a 5% NaOH aqueous solution, and further with 20 ml of water 3 times, and then dried by means of anhydrous sodium sulfate. The solvent was distilled off from the dried solution under vacuum to obtain 26.1 g (yield: 57%) of crude 1-methoxy-1-(1,1-dimethylethylperoxy)cyclohexane having a purity of 89%. The resulting crude peroxyketal was distilled at 40°-45° C. under a vacuum of 1 mmHg to obtain a purified peroxyketal having a purity of 99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05004780
Source datasetuspto-grants-1991_04
ORD IDord-c2c6505f94894b7f8d5baf77c0996f38
Source noteuspto-grants-1991_04