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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646809Generated: October 30, 2026

1-Phenethylpiperazine → HCID 15230865, compound

https://huagongshe.com/reaction/1646809

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenethylpiperazineHCID 79214—
ReactantHCID 19088025HCID 19088025—
SolventDichloromethaneHCID 6344—
ProductHCID 15230865HCID 1523086592.2%

Reaction Steps

A solution of p-nitrophenyl 7-(3,5,6-trimethyl-1,4-benzoquinon-2-yl)-7-phenyl-heptanoate (0.50 g, 1.05 mmoles) and 4-(2-phenylethyl)piperazine (0.20 g, 1.05 mmoles) in dichloromethane was allowed to stand at room temperature under stirring for 18 hours. After the solvent was evaporated in a reduced pressure, the residue was dissolved in ethylacetate and the solution was washed with aqueous potassium carbonate and water, and dried over magnesium sulfate. The solvent was evaporated and the residue was chromatographed on silica gel column with ethylacetate followed by chloroform-methanol (10:1) as eluant to give 4-[7-(3,5,6-trimethyl-1,4-benzoquinon-2-yl)-7-phenylheptanoyl]-(2-phenylethyl)piperazine (0.51 g, 92%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180742
Source datasetuspto-grants-1993_01
ORD IDord-6e7d53bfc6094815908a5c739c88dea1
Source noteuspto-grants-1993_01