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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 51298Erstellt: 24. Oktober 2026

Phenethyl bromide → 1-Phenethyl-1H-imidazole-4-carbaldehyde

https://huagongshe.com/de/reaction/51298

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenethyl bromideHCID 7666—
EduktSodium hydrideHCID 24758—
Edukt1H-Imidazole-4-carbaldehydeHCID 76428—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Phenethyl-1H-imidazole-4-carbaldehydeHCID 22289872—

Reaktionsschritte

Imidazole-4-carboxaldehyde (6.73 g, 70 mmol) was added portionwise to a suspension of sodium hydride (1.68 g, 60% dispersion in mineral oil, 70 mmol) in tetrahydrofuran (280 ml), and the mixture was then stirred at room temperature for 30 minutes. (2-Bromoethyl)benzene (9.56 ml, 70 mmol) was added, and the mixture was stirred at room temperature for 72 hours. The mixture was evaporated under reduced pressure and the residue was partitioned between water (300 ml) and dichloromethane (500 ml), and the layers were separated. The organic phase was dried (MgSO4) and evaporated under reduced pressure. The crude product was pre-adsorbed onto silica gel, and purified by column chromatography on silica gel using an elution gradient of ethyl acetate:pentane (50:50 to 100:0) to afford the title compound, 1.44 g. 1H-NMR (CDCl3, 400 MHz) δ: 3.16 (t, 2H), 4.23 (t, 2H), 7.02 (d, 2H), 7.28 (m, 3H), 7.36 (s, 1H), 7.50 (s, 1H), 9.83 (s, 1H). LRMS: m/z (ES+) 223 [MNa+].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713496B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-31441750fe72498fa9d8520b043eb1a1
Quellennotizuspto-grants-2004_03