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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 734479Erstellt: 23. Oktober 2026

Triethylamine → (1-Benzyl-1H-imidazol-2-yl)(2-bromo-3-methylphenyl)methanone

https://huagongshe.com/de/reaction/734479

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktThionyl ChlorideHCID 24386—
Edukt1-BenzylimidazoleHCID 77918—
Edukt2-Bromo-3-methylbenzoic acidHCID 2735588—
LösungsmittelAcetonitrileHCID 6342—
Produkt(1-Benzyl-1H-imidazol-2-yl)(2-bromo-3-methylphenyl)methanoneHCID 66771155102,3%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A solution of 2-bromo-3-methylbenzoic acid (2.0 g, 9.3 mmol) in thionyl chloride (4.75 ml, 65.1 mmol) was heated at 65° C., under nitrogen, for 3 h. The mixture was concentrated in vacuo and to the residue was added acetonitrile (25 ml). This solution was concentrated in vacuo and the process was repeated. To the final residue was added acetonitrile (25 ml), 1-benzylimidazole (1.62 g, 10.2 mmol) and triethylamine (1.44 ml, 10.2 mmol) and the reaction mixture was heated at 60° C., under nitrogen, for 18 h. The mixture was concentrated in vacuo and to the residue was added ethyl acetate (80 ml). The solution was washed with water (40 ml) and saturated aqueous sodium hydrogen carbonate solution (40 ml), dried (MgSO4) and concentrated in vacuo to give the title compound (3.38 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07592362B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-b3e311d636bc4019bca38db43e9304ee
Quellennotizuspto-grants-2009_09