HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 735363Erstellt: 25. Oktober 2026
N,N'-Dimethylethylenediamine → 4-Iodo-1H-benzimidazole
https://huagongshe.com/reaction/735363
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Edukt | 4-Bromo-1H-benzimidazole | HCID 11252584 | — |
| Edukt | Sodium iodide dihydrate | HCID 23685997 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Lösungsmittel | Ammonia | HCID 222 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 4-Iodo-1H-benzimidazole | HCID 21099512 | 155,9% |
Reaktionsschritte
Two reactions were set up as follows: A mixture of 4-bromo-1H-benzimidazole (725 mg, 3.68 mmol), sodium iodide dihydrate (1.37 g, 7.36 mmol), copper(I) iodide (70 mg, 0.37 mmol) and N,N′-dimethylethylenediamine (78 μL, 65 mg, 0.74 mmol) in dioxane (8 mL) was irradiated at 150° C. in a microwave reactor for 2.5 hours. The two reaction mixtures were combined, diluted with water (90 mL) and conc. ammonia (20 mL), then extracted with ethyl acetate (3×50 mL). The combined organic layers were washed with water (20 mL), then with saturated sodium chloride solution (50 mL), dried (MgSO4) and concentrated in vacuo. The crude product was purified by flash chromatography on silica gel, eluting with ethyl acetate, yielding the product as a yellow-white solid (1.40 g, 78%). 1H NMR (400 MHz, d6-DMSO): δ 12.72 (1H, s), 8.28 (1H, s), 7.61-7.53 (2H, m), 7.01 (1H, t, J=7.8 Hz); m/z (ES+) 245 [MH+].
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07592456B2 |
|---|
| Quelldatensatz | uspto-grants-2009_09 |
|---|
| ORD ID | ord-4419d7907f4c40be8385cea827892086 |
|---|
| Quellennotiz | uspto-grants-2009_09 |
|---|