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HRID 265358Erstellt: 23. Oktober 2026

Water → 1-(6-Ethoxy-carbonylhexyl)-2,4,5-triphenylimidazole

https://huagongshe.com/de/reaction/265358

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktDimethylformamideHCID 6228—
Edukt2,4,5-TriphenylimidazoleHCID 10232—
EduktSodium hydrideHCID 24758—
EduktEthyl 7-bromoheptanoateHCID 122490—
Produkt1-(6-Ethoxy-carbonylhexyl)-2,4,5-triphenylimidazoleHCID 8675107841%

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

2,4,5-Triphenylimidazole (1.3 g) was added to a suspension of sodium hydride (0.23 g) (50% dispersion in oil, washed with hexane) in dry dimethylformamide (40 ml) under nitrogen. The reaction was stirred at 45° C. for 1.5 h, cooled and ethyl 7-bromoheptanoate (1.1 g) in dry dimethylformamide (10 ml) was added. The reaction was stirred at 50° C. for 5 h, cooled and water was carefully added. The solvent was removed in vacuo and the residue was dissolved in ethyl acetate (100 ml). The organic solution was washed with saturated sodium chloride solution (150 ml), water (100 ml), dried over anhydrous magnesium sulphate and evaporated to dryness in vacuo. The residue was chromatographed on silica gel eluted with a dichloro-methane:ethanol gradient to give 1-(6-ethoxy-carbonylhexyl)-2,4,5-triphenylimidazole (0.81 g, 41%) as an oil. Found: C, 79.74; H, 7.32; N, 6.12%; C30H32N2O2 requires: C, 79.61; H, 7.13; N, 6.19%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05648373
Quelldatensatzuspto-grants-1997_07
ORD IDord-023f70a95cd24f09809a91d2f82fcf73
Quellennotizuspto-grants-1997_07