HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1,4-Dibenzylpiperazin-2-yl)-N,N-dimethylmethanamine → N,N-dimethyl-2-piperazinemethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1,4-Dibenzylpiperazin-2-yl)-N,N-dimethylmethanamine | HCID 14664170 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | N,N-dimethyl-2-piperazinemethanamine | HCID 14664185 | — |
Reaction Steps
A 4.7 g portion of 2-dimethylaminomethyl-1,4-bis(phenylmethyl)piperazine was dissolved in a mixture of 50 ml of ethanol, 20 ml of cyclohexane and 10 ml of glacial acetic acid. A 2.0 g portion of 10% palladium on carbon was added, the mixture was refluxed overnight and then filtered. The filtrate was evaporated, 5 ml of saturated aqueous potassium bicarbonate was added to the residue and this was extracted several times with dichloromethane. The extracts were combined, dried, filtered and evaporated, giving a gum which solidified on standing, giving 1.02 g of N,N-dimethyl-2-piperazinemethanamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05210193 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-f962c2fba81642c2a6d4365241e98f34 |
| Source note | uspto-grants-1993_05 |