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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051014Generated: November 1, 2026

Piperazine → (2-Fluoro-phenyl)-piperazin-1-yl-methanone

https://huagongshe.com/reaction/2051014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantTriethylamineHCID 8471—
ReactantPotassium CarbonateHCID 11430—
Reactant2-fluoro-N-phenylbenzenecarbohydrazonoyl chlorideHCID 72745343—
SolventChloroformHCID 6212—
ProductPhenylhydrazineHCID 7516—
Product(2-Fluoro-phenyl)-piperazin-1-yl-methanoneHCID 54486255.8%

Reaction Steps

To a stirred mixture of 12.5 parts of piperazine, 3.6 parts of N,N-diethylethanamine and 75 parts of trichloromethane was added a solution of 9 parts of 2-fluoro-N-phenylbenzenecarbohydrazonoyl chloride in 75 parts of trichloromethane. The whole was stirred for 2 hours at room temperature. After the addition of 5 parts of potassium carbonate, the reaction mixture was stirred for 30 minutes at reflux temperature. The mixture was cooled, washed with 100 parts of water and the layers were separated. The organic layer was dried, filtered and evaporated, yielding 6 parts (55.8%) of 1-(2-fluorobenzoyl)-piperazine, 2-phenylhydrazine as a residue (int. 9).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05015740
Source datasetuspto-grants-1991_05
ORD IDord-eb958c7b7c9e42df994cc17f1f8925ff
Source noteuspto-grants-1991_05