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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1395241Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1395241

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktBenzyl BromideHCID 7498—
EduktPotassium CarbonateHCID 11430—
Edukt1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]piperazineHCID 9974013—
Produkt1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-(phenylmethyl)piperazine maleateHCID 70573504—

Reaktionsschritte

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, 3.1 g (0.018) of benzylbromide were added dropwise at room temperature. The reaction mixture was then slowly heated and refluxed for 3 hours. Subsequently another 3.1 g (0.018 mol) of benzylbromide were added dropwise at room temperature. The mixture was refluxed for 1.5 hours, cooled and filtered. The solvent was distilled off and the residue was purified by column chromatography (silicagel) with a mixture of chloroform and ethyl acetate (1:1) as the eluent. A solution of maleic acid in diethyl ether was added to the desired eluate fraction, the precipitate was filtered off and crystallized from a mixture of methanol and dimethylformamide. 1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-(phenylmethyl)piperazine maleate (1:2) was obtained. Melting point 201.5°-202.5° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04202896
Quelldatensatzuspto-grants-1980_05
ORD IDord-aa8b25ce4ef744a2a03b81f1b6eb3abe
Quellennotizuspto-grants-1980_05