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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hexane | HCID 8058 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 4-(Imidazol-1-ylmethyl)benzonitrile | HCID 1236449 | — |
| Edukt | 1-(3-Bromopropyl)-4-fluorobenzene | HCID 14737133 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-[1-(4-cyanophenyl)4-(4-fluorophenyl)butyl]-1H-imidazole | HCID 9905115 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05962495 |
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| Quelldatensatz | uspto-grants-1999_10 |
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| ORD ID | ord-a37b8f5ca0db421ba5455d1607c863bc |
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| Quellennotiz | uspto-grants-1999_10 |
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