HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Benzylidenecyclohexanone → HCID 12118799, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Benzylidenecyclohexanone | HCID 98926 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 12118799 | HCID 12118799 | 88% |
| Product | Cyclohexanol, 2-(phenylmethyl)-, cis- | HCID 12283992 | — |
Reaction Steps
Then, 10 g of 2-benzylidenecyclohexanone were hydrogenated at room temperature using 1 g of Raney nickel in methanol under hydrogen pressure (3 kg/cm2) until the absorption of hydrogen was stopped. After an organic layer was collected by decantation and concentrated, the residue was purified by column chromatography, thereby obtaining 4.6 g of cis-2-benzylcyclohexanol and 4.4 g of trans-2-benzylcyclohexanol (yield: 88% in total).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05962403 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-66b69874a6dd4b8db91e126567b090d3 |
| Source note | uspto-grants-1999_10 |