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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287638Generated: October 31, 2026

1-(3-Chlorophenyl)piperazine → HCID 18705621, compound

https://huagongshe.com/reaction/2287638

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Chlorophenyl)piperazineHCID 1355—
ReactantSodium CarbonateHCID 10340—
Reactant2-NaphthylalanineHCID 185915—
Reactant1-(3-Chloropropyl)pyrrolidin-2-oneHCID 11105662—
SolventO-XyleneHCID 7237—
ProductHCID 18705621HCID 18705621—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 1-chloro-3-[2-oxopyrrolidin-1-yl]propane (1 g, 6.2 mmcl), 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 xylene (15 ml) was stirred at 150° C. for 14 hours. The solvent was removed at reduced pressure and residue was poured on water (30 ml). The separated residue was extracted with dichloromethane (2×25 ml), dried over Na2SO4 and concentrated to give 1-[4-(3-chlorophenyl)piperazin-1-yl]-3-[3-oxopyrrolidin-1-yl]propane as an oil which was purified by flash column chromatography over silica gel using chloroform as fluent, yield 0.72 g (36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06084097
Source datasetuspto-grants-2000_07
ORD IDord-bb60aef93cef40d1abc8470ffd372faf
Source noteuspto-grants-2000_07