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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 4317Erstellt: 25. Oktober 2026

1-Bromo-3-chloropropane → 1,3-Bis[4-(1-phenylethyl)-1-piperazinyl]propane tetrahydrochloride

https://huagongshe.com/reaction/4317

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-3-chloropropaneHCID 8006—
Edukt1-(1-Phenylethyl)piperazineHCID 2737134—
LösungsmittelEthanolHCID 702—
Produkt1,3-Bis[4-(1-phenylethyl)-1-piperazinyl]propane tetrahydrochlorideHCID 20152220211,9%

Reaktionsschritte

A mixture of 7.6 g of 1-(1-phenylethyl)piperazine, 3.2 g of 1-bromo-3-chloropropane and 50 ml of reagent ethanol was refluxed for 5 hours. The solvent was then removed under vacuum, 75 ml of water were added, and the mixture was extracted with ether (3×150 ml). The ether extract was evaporated to an oil and chromatographed on silica, the eluant being CH2Cl2 /CH3OH/ammonium hydroxide (45:5:1). The resulting yellow oil was dissolved in 150 ml of ether and precipitated with excess anhydrous hydrogen chloride to yield 6.1 g (51% of theory) of 1,3-bis[4-(1-phenylethyl) -1-piperazinyl]propane tetrahydrochloride. The product was recrystallized from ethanol/water to yield a white crystalline solid (m.p. 236°-246° C., with decomp.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04725597
Quelldatensatzuspto-grants-1988_02
ORD IDord-17ee4450157049288fbf93d876e000e4
Quellennotizuspto-grants-1988_02