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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649512Generated: November 1, 2026

1-Benzylpiperazine → HCID 20480158, compound

https://huagongshe.com/reaction/1649512

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BenzylpiperazineHCID 75994—
ReactantHCID 12802913HCID 12802913—
SolventAcetonitrileHCID 6342—
ProductHCID 20480158HCID 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 dihydrochloric salt affords 1-[2-(4-benzoylphenyl)propyl]piperazine dihydrochloride m.p. 243°-245° C. (from ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04417052
Source datasetuspto-grants-1983_11
ORD IDord-3ddc4e34cb404ce3907a457d4c30a1cf
Source noteuspto-grants-1983_11