Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395240Generated: October 25, 2026

Ethanol → 1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine maleate

https://huagongshe.com/reaction/1395240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
Reactant(3-Bromopropyl)benzeneHCID 12503—
Reactant1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]piperazineHCID 9974013—
Product1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine maleateHCID 25009462—

Reaction Steps

To a mixture of 6 g (0.018 mol) of 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]piperazine (prepared as described in Example 3) and 3 g of potassium carbonate powder in 50 ml of ethanol, 3.6 g (0.018 mol) of (3-bromopropyl) benzene (G.O. Aspinall et al., J.Chem.Soc.1950, 743) was added dropwise at room temperature. The mixture was then slowly heated and refluxed for 3 hours. The reaction mixture was filtered and the filtrate was concentrated. The residue was taken up in diethyl ether, undissolved matter was filtered off and ethereal maleic acid was added until the liquid reacted acidic. The precipitate was filtered off and crystallized from a mixture of methanol and dimethylformamide. 1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine maleate (1:2) was obtained. Melting point 185.0°-185.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04202896
Source datasetuspto-grants-1980_05
ORD IDord-10f2db6e61094661942ede8a07b2279d
Source noteuspto-grants-1980_05