HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 23282592, compound → HCID 23282594, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 23282592 | HCID 23282592 | — |
| Catalyst | HCID 178502593 | HCID 178502593 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23282594 | HCID 23282594 | 57.2% |
Reaction Steps
To a solution of 4-(3,4-dimethyl-1-piperazinyl)-1-benzylpiperidine (4.2 g) in ethanol (50 ml) is added 20% palladium hydroxide-carbon (0.4 g), and the mixture is subjected to catalytic hydrogenation at 50° C. under atmospheric pressure. The catalyst is removed by filtration, and the filtrate is concentrated under reduced pressure. The residue is evaporated to give 4-(3,4-dimethyl-1-piperazinyl)piperidine (1.65 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06140330 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-8ab3fcdc4262446a958e9ff38127cb79 |
| Source note | uspto-grants-2000_10 |