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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2229801Erstellt: 25. Oktober 2026

Potassium Carbonate → 2,5-Pyrrolidinedione, 1-[3-[4-(2-methoxyphenyl)-1-piperazinyl]propyl]-

https://huagongshe.com/reaction/2229801

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktSuccinimideHCID 11439—
Edukt1-(3-Chloropropyl)-4-(2-methoxyphenyl)piperazineHCID 622669—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelAcetoneHCID 180—
Produkt2,5-Pyrrolidinedione, 1-[3-[4-(2-methoxyphenyl)-1-piperazinyl]propyl]-HCID 9949436—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Scheme-I: A mixture of 2,5-dioxopyrrolidine (3.68 g, 37.24 mmol), 1-[4-(2-methoxyphenyl)-piperazin-1-yl]-3-chloropropane (10.0 g, 37.24 mmol), potassium carbonate (7.70 g, 55.8 mmol) and tetrabutylammonium bromide (2.38 g, 7.4 mmol) in acetone (100 ml) was refluxed for 12 hours at 80° C. with stirring. The solvent was evaporated off in vacuo and the residue was taken up in water (80 ml). The aqueous solution was extracted with chloroform (3×50 ml) and the organic layers combined, washed with water (2×50 ml); dried over Na2SO4 and evaporated in vacuo to give the title compound. The product was purified by column chromatography over flash silica gel using chloroform-methanol (99:1) as eluent; yield 8.00 g (65%) in oil. The hydrochloride salt was prepared by the method described above; mp 199-202° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06420559B1
Quelldatensatzuspto-grants-2002_07
ORD IDord-b17891d1bb4e4b2aa467c1957a317127
Quellennotizuspto-grants-2002_07