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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464513Generated: October 28, 2026

1-Phenethylpiperazine → HCID 15230865, compound

https://huagongshe.com/reaction/1464513

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 numberUS05304658
Source datasetuspto-grants-1994_04
ORD IDord-2f6464b38ccb49278881e02444fb9f5b
Source noteuspto-grants-1994_04