HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Propylcyclohexanone → HCID 178439285, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Propylcyclohexanone | HCID 142482 | — |
| Reactant | HCID 178439119 | HCID 178439119 | — |
| Reactant | HCID 178439192 | HCID 178439192 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 178439285 | HCID 178439285 | — |
Reaction Steps
A solution in 300 ml of cyclohexane of 24.8 g of 1-(trans-4-propylcyclohexyl)-4-propylcyclohexene [obtainable by reacting 4-propylcyclohexanone with 4-propylcyclohexylmagnesium bromide to give 1-(trans-4-propylcyclohexyl)-4-propylcyclohexanol and dehydrating the latter] is hydrogenated over 4 g of 10% PdC at 20° and 1 bar until absorption of H2 ceases. The mixture is filtered and worked up analogously to Example 3 via the thiourea adduct to give trans,trans-4,4'-dipropylbicyclohexyl, c.p. 41°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04868341 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-3bc7e026ed984b50bba04e5e31c43bae |
| Source note | uspto-grants-1989_09 |