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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 265361Erstellt: 25. Oktober 2026

Water → 1-(8-Bromooctyl)-2,4,5-triphenylimidazole

https://huagongshe.com/reaction/265361

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt2,4,5-TriphenylimidazoleHCID 10232—
EduktSodium hydrideHCID 24758—
Edukt1,8-DibromooctaneHCID 78310—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-(8-Bromooctyl)-2,4,5-triphenylimidazoleHCID 2291643750%

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

2,4,5-Triphenylimidazole (5 g) was added to a suspension of sodium hydride (1.0 g) (50% dispersion in oil, washed with hexane) in dry dimethylformamide (80 ml) under nitrogen. The reaction was stirred at 45° C. for 1 h, cooled and added, over 1 h to a solution of 1,8-dibromo-octane (30 g) in dry dimethylformamide (100 ml) under nitrogen. The reaction was stirred at room temperature for 24 h, water was carefully added and the solvent was removed in vacuo. The residue was dissolved in ethyl acetate (500 ml), washed with water (250 ml), 2N aqueous hydrochloric acid (250 ml), saturated sodium chloride solution (250 ml), dried over anhydrous magnesium sulphate and evaporated to dryness in vacuo. Distillation to remove 1,8-dibromooctane and chromatography on silica gel eluted with dichloromethane gave 1-(8-bromooctyl)-2,4,5-triphenylimidazole (4.1 g, 50%) as an oil; NMR d (CDCl3) 0.9-1.7 (12H, m, 6×CH2), 3.3 (2H, t, BrCH2), 3.9 (2H, t, N--CH2), 7.1-7.7(15H, m, 3×Ph) ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05648373
Quelldatensatzuspto-grants-1997_07
ORD IDord-711ec5d42d0d4235916d1f906fd9f1f0
Quellennotizuspto-grants-1997_07