HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Cyclohexen-1-one, 3,5-dimethyl-4-(3-methyl-2-buten-1-yl)- → Cyclohexanone, 3,5-dimethyl-4-(3-methyl-2-buten-1-yl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Cyclohexen-1-one, 3,5-dimethyl-4-(3-methyl-2-buten-1-yl)- | HCID 93696 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | Cyclohexanone, 3,5-dimethyl-4-(3-methyl-2-buten-1-yl)- | HCID 20469263 | 87.4% |
Reaction Steps
A solution of 3,5-dimethyl-4-(3-methyl-2-butenyl)-2-cyclohexen-1-one (8.2 g, 0.043 mol) in 0.3 M ethanolic KOH (16 mL) was hydrogenated at room temperature and 1 atmosphere over 5% palladium on carbon (0.8 g). After uptake of 1 equivalent of hydrogen, the solution was filtered through Celite and concentrated. The residue was partitioned between hexane and water; then the hexane layer was dried (Na2SO4) and the solvent removed on a rotary evaporator. Kugelrohr distillation gave 7.3 g of 3,5-dimethyl-4-(3-methyl-2-butenyl) cyclohexanone, bp 115° C./0.5 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04326996 |
| Source dataset | uspto-grants-1982_04 |
| ORD ID | ord-90c556e4443d4828b49119ceb5ec21c7 |
| Source note | uspto-grants-1982_04 |