HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 22494617, compound → HCID 22494683, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 22494617 | HCID 22494617 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22494683 | HCID 22494683 | 75.7% |
Reaction Steps
A mixture of crude 1-acetyl-4-[4-[3-(2-cyclohexen-1-yloxy)propyloxy]phenyl]piperazine (1.55 g) in ethanol (16 ml) was hydrogenated at atmospheric pressure with 10% palladium-carbon (0.16 g) for 5 hours. After removal of catalyst by filtration, the filtrate was concentrated in vacuo to give crude 1-acetyl-4-[4-(3-cyclohexyloxypropyloxy)phenyl]piperazine (1.18 g), that was used in the next reaction directly, as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06884868B1 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-c0fa1bda83ae4f2cace21f1d3474b299 |
| Source note | uspto-grants-2005_04 |