HuagongsheHuagongshe Chemistry Print Report · For research reference only
4,4-dipropylcyclohex-2-en-1-one → 4,4-dipropylcyclohexan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4,4-dipropylcyclohex-2-en-1-one | HCID 4450494 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4,4-dipropylcyclohexan-1-one | HCID 2775995 | 98% |
Reaction Steps
To a suspension of 10% palladium on carbon (0.1 equivalents) in ethyl acetate was added 4,4 dipropylcyclohex-2-enone, prepared as described in Example 3. The reaction mixture was hydrogenated at 300N/m2 hydrogen in a Parr hydrogenation apparatus at room temperature until hydrogen uptake has ceased (0.5-5 hours). The catalyst was removed by filtration through celite and the filtrate was concentrated to give the desired product as a colorless oil. The product was used without further purification. Yield 98%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04963557 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-2f69d15c3a9647d48aec352dd41204ac |
| Source note | uspto-grants-1990_10 |