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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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phthalic Anhydride | HCID 6811 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2-(2-Aminoethyl)benzimidazole dihydrochloride | HCID 2788071 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-(2-(1H-Benzo[d]imidazol-2-yl)ethyl)isoindoline-1,3-dione | HCID 3352112 | 71,4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06984642B1 |
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| Quelldatensatz | uspto-grants-2006_01 |
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| ORD ID | ord-c13ace95260645c7905fe54833e5850b |
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| Quellennotiz | uspto-grants-2006_01 |
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