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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416262Generated: November 1, 2026

Piperazine → HCID 19367121, compound

https://huagongshe.com/reaction/1416262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant2,5-DifluorobenzonitrileHCID 123558—
SolventDimethylformamideHCID 6228—
ProductHCID 19367121HCID 1936712145.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of piperazine (Aldrich; 1.28 g), 2,5-difluorobenzonitrile (Lancaster; 0.422 g), and DMF (4 mL) is stirred at 80° C. for 1.5 h, after which the mixture is cooled and partitioned between dichloromethane, water, and aq. sodium bicarbonate. The organic layers are dried over sodium sulfate, concentrated, and the residue is crystallized from dichloromethane/ethyl ether/hexane to give 0.282 g of 5-fluoro-2-(piperazin-1-yl)benzonitrile; mp 83-83.5° C.; 1H NMR (CDCl3) δ3.10, 7.00, 7.21, 7.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05912246
Source datasetuspto-grants-1999_06
ORD IDord-43a9b9c6af194a7a97bc1e25dd708430
Source noteuspto-grants-1999_06