HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → Cyclohexanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | 1,2-Dichlorobenzene | HCID 7239 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Cyclohexanol | HCID 7966 | — |
| Product | Cyclohexanone | HCID 7967 | — |
| Product | Cyclohexyl hydroperoxide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09024076B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-3106ce0eb18147379849d36e5eceb626 |
| Source note | uspto-grants-2015_05 |