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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463302Generated: October 29, 2026

1-(4-Fluorophenyl)piperazine → HCID 13073853, compound

https://huagongshe.com/reaction/463302

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Fluorophenyl)piperazineHCID 75260—
Reactant(Chloromethyl)cyclopropaneHCID 80013—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
ProductHCID 13073853HCID 13073853139.1%

Reaction Steps

To 50 ml of ethanol, are added 3.6 g (0.02 mole) of 1-(4-fluorophenyl)piperazine, 2.0 g (0.022 mole) of cyclopropylmethyl chloride, and 1.9 g (0.023 mole) of sodium bicarbonate. The mixture is kept refluxing for 7 hours while being stirred. After having been cooled, the reaction mixture is freed from inorganic matters by filtration and the filtrate is concentrated in vacuo. The residue is dissolved in diethyl ether and gaseous hydrogen chloride is introduced into the solution, while being cooled, to precipitate crystals which are collected by filtration. Upon recrystallization from ethanol there are obtained 4.7 g (77% yield) of 1-(cyclopropylmethyl)-4-(4-fluorophenyl)piperazine dihydrochloride melting at 153°-154° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04518712
Source datasetuspto-grants-1985_05
ORD IDord-29c73aadd0bd43c9a8f078aab1435bb0
Source noteuspto-grants-1985_05