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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378324Generated: October 25, 2026

1-Benzylpiperazine → 7-Methoxy-4-{[4-benzylpiperazinyl]methyl}chromen-2-one

https://huagongshe.com/reaction/1378324

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BenzylpiperazineHCID 75994—
Reactant4-Bromomethyl-7-methoxycoumarinHCID 121894—
ReactantPotassium BicarbonateHCID 516893—
SolventTetrahydrofuranHCID 8028—
Product7-Methoxy-4-{[4-benzylpiperazinyl]methyl}chromen-2-oneHCID 1106748—

Reaction Steps

0.03 mol of 1-benzylpiperazine, 0.03 mol of 7-methoxy-2-oxo-4-bromomethyl-3-chromene and 0.03 mol of potassium bicarbonate are introduced into an Erlenmeyer flask containing 150 ml of tetrahydrofuran. The mixture is brought to reflux for 24 hours. The reaction is brought to an end and, after cooling, the solution is filtered and evaporated under reduced pressure. The residue is then purified by chromatography on a column of silica gel, methylene chloride generally being used as eluent. The final product is thus obtained in the base form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05668138
Source datasetuspto-grants-1997_09
ORD IDord-5b36025d051f46c293507735243774b2
Source noteuspto-grants-1997_09