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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728813Generated: October 29, 2026

1-Benzyl-4-(4-nitrophenyl)piperazine → 4-(4-Benzylpiperazin-1-yl)aniline

https://huagongshe.com/reaction/728813

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-(4-nitrophenyl)piperazineHCID 2747427—
ReactantTin tetrachloride dihydrateHCID 85782573—
SolventEthanolHCID 702—
Product4-(4-Benzylpiperazin-1-yl)anilineHCID 737259—

Reaction Steps

Add 474 g (2.10 mol) tin chloride dihydrate to a refluxing solution of 125 g (0.420 mol) 4-(4-nitrophenyl)-1-(phenylmethyl)piperazine in ethanol. Reflux the solution for about 15 h then cool to room temperature and remove the solvent. Dissolve the residue in water and adjust to pH 12 withsodium hydroxide. Extract the aqueous solution with methylene chloride and dry the organic layer with anhydrous sodium sulfate. Concentration at reduced pressure gives the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05051423
Source datasetuspto-grants-1991_09
ORD IDord-a6e88dd3930a417ea6dae43e11ad4dec
Source noteuspto-grants-1991_09