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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727175Generated: November 2, 2026

Cyclopentanecarbonyl chloride → 1-Cyclopentanecarbonylpiperazine

https://huagongshe.com/reaction/1727175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentanecarbonyl chlorideHCID 78284—
ReactantPiperazine, hexahydrateHCID 120181—
SolventEthanolHCID 702—
Product1-CyclopentanecarbonylpiperazineHCID 15512779—

Reaction Steps

Piperazine hexahydrate (8.55 g, 44.0 mmol) was dissolved in absolute ethanol (50 ml) and then refluxed for 10 min. Cyclopentanecarbonyl chloride (5.83 g, 44 mmol) was added dropwise at 65° C. and the reaction mixture was refluxed for 30 min and then stirred at room temperature for 18 h. The reaction mixture was cooled, filtered and the filtrate was concentrated in vacuo to give ˜20 ml of solution. The concentrate was cooled and then filtered again. Ethanolic hydrogen chloride was added to the mother liquor, and the reaction mixture was concentrated to give a white solid, which was dissolved in water (15 ml). The solution was basified to pH 14 and the product was extracted with dichloromethane (7×50 ml). The extracts were dried, (Na2SO4) and concentrated to give the title compound as a yellowish residue, which was distilled to give the product (1.28 g, 7.0 mmol, 16%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07494992B2
Source datasetuspto-grants-2009_02
ORD IDord-5d00533441384f46bb124744605133f2
Source noteuspto-grants-2009_02