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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1737858Erstellt: 26. Oktober 2026

Hexane → 1-[1-(4-cyanophenyl)4-(4-fluorophenyl)butyl]-1H-imidazole

https://huagongshe.com/reaction/1737858

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
EduktAmmonium ChlorideHCID 25517—
Edukt4-(Imidazol-1-ylmethyl)benzonitrileHCID 1236449—
Edukt1-(3-Bromopropyl)-4-fluorobenzeneHCID 14737133—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-[1-(4-cyanophenyl)4-(4-fluorophenyl)butyl]-1H-imidazoleHCID 9905115—

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

1-(4-cyanobenzyl)-imidazole (1 g, 0.0054 mol) is dissolved into dry tetrahydrofuran (30 ml) and cooled to -70° C. n-BuLi in hexane (0.0054 mol) is added dropwise into the reaction mixture. After stirring for additional 30 min at -70° C. 3-(4-fluorophenyl)propyl bromide (1.5 g, 0.0069 mol) in THF (10 ml) is added to the mixture and stirig is continued for 2 hours. Then the mixture is allowed to warm to room temperature. Saturted aqueous ammonium chloride solution is added to the mixture, shaked and then the layers are separated. THF-phase is dried and evaporated to dryness. The residue is crystalizd from isopropanol as hydrogen chloride salt. The filtrate is purified by flash chromatography.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05962495
Quelldatensatzuspto-grants-1999_10
ORD IDord-a37b8f5ca0db421ba5455d1607c863bc
Quellennotizuspto-grants-1999_10