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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287637Generated: October 31, 2026

1-(3-Chlorophenyl)piperazine → 1-[4-(3-Chlorophenyl)piperazin-1-yl]-3-[2-oxopyrrolidin-1-yl]propane

https://huagongshe.com/reaction/2287637

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Chlorophenyl)piperazineHCID 1355—
ReactantSodium CarbonateHCID 10340—
Reactant2-NaphthylalanineHCID 185915—
Reactant1-(3-Chloropropyl)pyrrolidin-2-oneHCID 11105662—
SolventTolueneHCID 1140—
Product1-[4-(3-Chlorophenyl)piperazin-1-yl]-3-[2-oxopyrrolidin-1-yl]propaneHCID 9927143—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 1-chloro-3-[2-oxopyrrolidin-1-yl]propane (1.0 g, 6.2 mmol), 1-(3-chlorophenyl)piperazine (1.22 g, 6.2 minol), anhydrous Na2CO3 (0.33 g, 3.1 mmol) and Nal (0.093 g, 0.6 mmcl) in dry toluene (10 ml) was stirred at 110° C. for 12 hrs. The solvent was removed at reduced pressure and residue was poured on water (20 ml). The separated residue was extracted with ethylacetate (3×20 ml), dried over Na2SO4 and concentrated under reduced pressure to give 1-[4-(3-chlorophenyl)piperazin-1-yl]-3-[2-oxopyrrolidin-1-yl]propane as an oil which was purified by flash column chromatography over silica gel using chloroform as eluent, yield 0.60 g (30.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06084097
Source datasetuspto-grants-2000_07
ORD IDord-66e46727068041e69d7ff37eee4ce067
Source noteuspto-grants-2000_07