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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942405Generated: November 3, 2026

1-Phenylpiperazine → 5-Hydroxy-1-(4-phenylpiperazin-1-yl)pentan-1-one

https://huagongshe.com/reaction/1942405

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantTriethylamineHCID 8471—
ReactantDelta-ValerolactoneHCID 10953—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichloroethaneHCID 11—
Solvent1,1-DichloroethaneHCID 6365—
Product5-Hydroxy-1-(4-phenylpiperazin-1-yl)pentan-1-oneHCID 66937601—

Reaction Steps

A solution of 5.4 mL (37.5 mmol) Et3N in 10 ml, 2-dichloroethane was added drop by drop under ice cooling to a suspension of 3.70 g (27.5 mmol) AlCl3 in 20mL dichloroethane. At room temperature a solution of 4.21 ml (27.5 mmol) 1-phenylpiperazine and 2.32 mL (25 mmol) delta-valerolactone in 15 mL 1,2-dichloroethane was added to the mixture. After one hour of stirring at room temperature the mixture was quenched with ice water and stirred for another 30 minutes. The suspension was filtered by Celite. After adding of dichloromethane, separating of the organic layer, washing it with water, drying it with Na2SO4 and evaporating of the solvent, followed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389555B2
Source datasetuspto-grants-2013_03
ORD IDord-3623fe177a8644d8a739693668af63b0
Source noteuspto-grants-2013_03