HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(4-Methoxyphenyl)-2-cyclohexen-1-one → 3-(4-Methoxyphenyl)cyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(4-Methoxyphenyl)-2-cyclohexen-1-one | HCID 367927 | — |
| Reactant | Cornforth reagent | HCID 2724130 | — |
| Reactant | pyridine TFA | HCID 9813011 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(4-Methoxyphenyl)cyclohexanone | HCID 11977050 | — |
Reaction Steps
1.5 g of 5% palladium on active carbon are added to 15.15 g of 3-(4-methoxyphenyl)-2-cyclohexen-1-one in 400 ml of methanol and stirring is carried out in a hydrogen atmosphere for 4 hours. The catalyst is filtered off and the reaction mixture is concentrated. The mixture so obtained is dissolved in 200 ml of dichloromethane and stirred with 26.9 g of pyridinium dichromate and 2.1 g of pyridinium trifluoroacetate at room temperature for 6 hours. The reaction mixture is decanted, concentrated and purified over silica gel. 3-(4-Methoxyphenyl)cyclohexanone is obtained in the form of a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07569727B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-b93427b7031f42fe9a2722fa8891c463 |
| Source note | uspto-grants-2009_08 |