Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 274691Erstellt: 25. Oktober 2026

1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)- → 4-(2-Phthalimidoethyloxy)pyridine

https://huagongshe.com/reaction/274691

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)-HCID 11325—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
EduktHCID 178418642HCID 178418642—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(2-Phthalimidoethyloxy)pyridineHCID 190792113,1%

Reaktionsschritte

To a solution of 4.76 g (50 mmol) of 4-hydroxypyridine and 13.97 g (55 mmol) of N-(2-bromoethyl)phthalimide in 80 ml of DMF, 8.23 ml (55 mmol) of 1,8-diazabicyclo[5.4.0]-7-undecene was added. The mixture was stirred at room temperature for 32 hours. After the solvent was distilled off, the mixture was poured into water and extracted with ethyl acetate. The mixture was washed with water and dried over anhydrous magnesium sulfate, and then the solvent was distilled off. The residue was purified by-column chromatography (eluent: ethyl acetate) to obtain 0.41 g of the desired compound (yield: 3.1%, colorless crystal).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05389658
Quelldatensatzuspto-grants-1995_02
ORD IDord-ade200c334424e03bcafaf1b365d2052
Quellennotizuspto-grants-1995_02