HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzylpiperazine → HCID 20480158, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | HCID 12802913 | HCID 12802913 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 20480158 | HCID 20480158 | — |
Reaction Steps
Reaction of 2-(4-benzoylphenyl)propyl p-toluenesulfonate with 1-benzylpiperazine in acetonitrile and isolation of the product in the form of the free base affords 1-[2-(4-benzoylphenyl)propyl]-4-benzylpiperazine. Conversion of the latter to the ethylene glycol ketal, catalytic reduction of the latter over palladium-on-charcoal at a hydrogen pressure of 50 p.s.i. in order to effect catalytic debenzylation thereof using the manipulative procedure described in Example 10 above, cleavage of the ketal with aqueous hydrochloric acid, and isolation of the product in the form of the dihydrochloride salt affords 1-[2-(4-benzoylphenyl)propyl]piperazine dihydrochloride, m.p. 243°-245° C. (from ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04308382 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-a15b4ea09ed2418aa7faadc299e30cbf |
| Source note | uspto-grants-1981_12 |