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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571168Generated: November 1, 2026

Hydrogen Peroxide → Cyclohexanol

https://huagongshe.com/reaction/571168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
Reactant1,2-DichlorobenzeneHCID 7239—
ReactantCyclohexaneHCID 8078—
SolventAcetonitrileHCID 6342—
ProductCyclohexanolHCID 7966—
ProductCyclohexanoneHCID 7967—
ProductCyclohexyl hydroperoxideHCID 69835—

Reaction Steps

Synthesize alkane oxidation catalyst in situ and oxidize alkane (cyclohexane) as follows. Add SiO2—C (3.3 mg, 0.6 groups/nm2) in acetonitrile (2 mL) and ([(C6H12N3R3)Mn2O3]Z2) (0.2 mM) to a container. The carboxylate group to Mn atom ratio is 0.50:1.0. Add o-dichlorobenzene (100 microliter (μL), 390 mmol) and cyclohexane (50 μL, 200 mmol) to the contents of container and maintain at 0° C. Add H2O2 (30 weight percent (wt %), 130 μL) to the contents of container. Seal the container and react to produce an alkane oxidation product (cyclohexanone (CyO), cyclohexanol (CyOH), and/or cyclohexyl hydroperoxide (Cy-OOH)). The concentrations of these species are determined as a function of time using gas chromatography and are shown in Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024076B2
Source datasetuspto-grants-2015_05
ORD IDord-3106ce0eb18147379849d36e5eceb626
Source noteuspto-grants-2015_05