Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084461Generated: October 26, 2026

1,1-Dimethoxycyclohexane → 1-Methoxy-1-[(2-methylbutan-2-yl)peroxy]cyclohexane

https://huagongshe.com/reaction/1084461

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DimethoxycyclohexaneHCID 13616—
Reactanttert-Amyl hydroperoxideHCID 76962—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventDimethyl SulfoxideHCID 679—
Product1-Methoxy-1-[(2-methylbutan-2-yl)peroxy]cyclohexaneHCID 1457303677.4%

Reaction Steps

A mixed solution consisting of 15.9 g of dimethyl sulfoxide and 1.2 g of p-toluenesulfonic acid was kept at 20° C., into which was added dropwise another solution consisting of 29.1 g of cyclohexanone-dimethylacetal and 21.1 g of 1,1-dimethylpropyl hydroperoxide. The resulting solution had an acid concentration of 0.1 mol/kg of the solution. The solution was treated in the same manner as described in Example 1 to obtain 33.8 g (yield: 67%) of crude 1-methoxy-1-(1,1-dimethylpropylperoxy)cyclohexane having a purity of 86%. The resulting crude peroxyketal was distilled at 43°-45° C. under a vacuum of 0.1 mmHg to obtain a purified peroxyketal having a purity of 98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05004780
Source datasetuspto-grants-1991_04
ORD IDord-894a0d2ba051497b83f47d4f19a68f62
Source noteuspto-grants-1991_04