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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 42279Erstellt: 23. Oktober 2026

Acetic Acid → 2-(3-fluorophenyl)-1H-imidazole

https://huagongshe.com/de/reaction/42279

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktHydrochloric AcidHCID 313—
Edukt3-FluorobenzonitrileHCID 67880—
EduktAminoacetaldehyde dimethyl acetalHCID 89728—
EduktSodium MethoxideHCID 10942334—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(3-fluorophenyl)-1H-imidazoleHCID 31681641%

Reaktionsschritte

In a flask containing 3-flourobenzonitrile (Matrix Scientific, 3.0 g, 25 mmol) was added methanol (30 mL) and sodium methoxide (Aldrich, 25% by wt. in methanol, 2.83 mL, 12.4 mmol). The reaction mixture was stirred for 1.5 hours and aminoacetaldehyde dimethyl acetal (Alfa Aesar, 2.60 g, 24.8 mmol) and acetic acid (2.83 mL, 49.5 mmol) were subsequently added and the solution was heated at reflux for one hour. After cooling to room temperature, methanol (25 mL) and 6 N HCl (8 mL) was added and the solution was heated at reflux for 16 hours. After cooling the solution to room temperature the residue was taken up in a 1:1 mixture (v/v) of water and ethyl acetate (50 mL). The aqueous layer was separated and the pH of this solution was adjusted to pH 9 with 2 N NaOH, upon which a white precipitate formed in solution. The solid was collected by filtration and dried under high vacuum to provide 2-(3-fluorophenyl)-1H-imidazole as an off-white solid (1.67 g, 41% yield, MS (ESI+) m/z 163.1 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536185B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-d07c9840b9234973930b2cb4f8b36d18
Quellennotizuspto-grants-2013_09