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HRID 1610794Erstellt: 25. Oktober 2026

Phthalic Anhydride → 2-(2-(1H-Benzo[d]imidazol-2-yl)ethyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/1610794

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhthalic AnhydrideHCID 6811—
EduktTriethylamineHCID 8471—
Edukt2-(2-Aminoethyl)benzimidazole dihydrochlorideHCID 2788071—
LösungsmittelChloroformHCID 6212—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(2-(1H-Benzo[d]imidazol-2-yl)ethyl)isoindoline-1,3-dioneHCID 335211271,4%

Reaktionsschritte

2-Aminoethylbenzimidazole dihydrochloride (Bull. Soc. Chim. Fr. 1991, 128, 255-259; 2.34 g, 10 mmol), phthalic anhydride (1.63 g, 11 mmol) and triethylamine (2.79 ml, 20 mmol) in chloroform (25 ml) were heated at reflux overnight, and the mixture was then cooled to room temperature, diluted with ethyl acetate and filtered off. The filtrate was washed with saturated sodium carbonate solution, buffer (pH=7) and saturated sodium chloride solution and dried over sodium sulphate. Chromatography (dichloromethane:methanol 10:1, Rf=0.4) gave 2.08 g of 2-(2-phthalimidylethyl)-benzimidazole (71.4% of theory) as a colourless foam. MS (DCI, NH3)=292 (M+H+). 1H-NMR (DMSO-d6): 3.15 (2H, t); 4.0 (2H, t); 7.05-7.2 (2H, m); 7.4-7.5 (2H, m); 7.8-7.9 (4H, m); 12.4 (1H, br s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06984642B1
Quelldatensatzuspto-grants-2006_01
ORD IDord-c13ace95260645c7905fe54833e5850b
Quellennotizuspto-grants-2006_01