HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methoxycyclohexanol (cis,trans) → 4-Methoxycyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methoxycyclohexanol (cis,trans) | HCID 140332 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Methoxycyclohexanone | HCID 535028 | — |
Reaction Steps
4-Methoxycyclohexanol (2.0 g, 15.0 mmol) was taken up in 150 mL of DCM. Pyridinium chlorochromate (5.0 g, 23.0 mmol) was added. After 60 hours, the mixture was filtered through a plug of Florisil and concentrated under reduced pressure. The residue was taken up in 50 mL of ether and filtered through a plug of silica gel. The solvent was removed under reduced pressure, affording 4-methoxycyclohexanone as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08053438B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-f507dd16125c411db6001cdd6e80706a |
| Source note | uspto-grants-2011_11 |