Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 373821Erstellt: 24. Oktober 2026

Carbon Dioxide → 1-(7-Methoxy-1-naphthyl)-4-benzyl-2,6-piperazinedione

https://huagongshe.com/de/reaction/373821

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
EduktN-Benzylaminodiacetic acidHCID 77606—
Edukt7-Methoxynaphthalen-1-amineHCID 235817—
LösungsmittelEthanolHCID 702—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(7-Methoxy-1-naphthyl)-4-benzyl-2,6-piperazinedioneHCID 1980848782%

Reaktionsschritte

126 mmol (2.2 equivalents) of carbonyldiimidazole are added to a suspension containing 58 mmol (1 equivalent) of N-benzyliminodiacetic acid in 200 ml of anhydrous tetrahydrofuran. The mixture is brought to reflux until the evolution of CO2 has ceased. A solution containing 58 mmol (1 equivalent) of 1-amino-7-methoxynaphthalene in 40 ml of anhydrous tetrahydrofuran is then added to the above mixture. The resulting mixture is brought to reflux for 20 hours, the solvent is evaporated off and the residue obtained is taken up with 300 ml of anhydrous ethanol. The precipitate formed is filtered off and then dissolved in 200 ml of dichloromethane. The insoluble matter is filtered off and the filtrate concentrated. The expected product is then obtained after taking up in isopropyl ether followed by filtration.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05166156
Quelldatensatzuspto-grants-1992_11
ORD IDord-0f62f74f5ae2418196acafa38547bcb3
Quellennotizuspto-grants-1992_11