HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → N-cyclohexyloxy-4-oxo-2,2,6,6-tetramethylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | 1-Hydroxy-2,2,6,6-tetramethyl-4-oxopiperidine | HCID 98642 | — |
| Catalyst | Ferrous sulfate heptahydrate | HCID 62662 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-cyclohexyloxy-4-oxo-2,2,6,6-tetramethylpiperidine | HCID 22019868 | 35% |
Reaction Steps
A solution of 20.1 g (0.295 mol) of 50% aqueous hydrogen peroxide is added over 6 hours at 60° C. to a mixture of 8.51 g (50.0 mmol) of 1-oxyl-2,2,6,6-tetramethylpiperid-4-one, 0.70 g (2.5 mmol) of iron(II) sulfate heptahydrate, 0.3 ml (5 mmol) of methanesulfonic acid, 11 ml of cyclohexane, and 90 ml of methanol. Shortly after the addition is completed, the reaction mixture tests negative for hydrogen peroxide. The reaction mixture is concentrated to afford 4.4 g (35% yield) of the title compound, isolated as a yellow oil. Structure is confirmed by mass spectrometry and NMR analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07390904B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-a53408cb0ce54faa8f117c9a7ef781f0 |
| Source note | uspto-grants-2008_06 |