HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1885831Erstellt: 26. Oktober 2026
Triethylamine → 4-Phenyl-1-(phenylmethyl)-1H-imidazole-2-carbonitrile
https://huagongshe.com/reaction/1885831
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Cyanogen Chloride | HCID 10477 | — |
| Edukt | 1H-Imidazole, 4-phenyl-1-(phenylmethyl)- | HCID 2927458 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 4-Phenyl-1-(phenylmethyl)-1H-imidazole-2-carbonitrile | HCID 19877957 | — |
Reaktionsschritte
Under nitrogen, 2.0 g (0.0325 ml) cyanogen chloride was added to a 5° C. solution of 6.0 g (0.0256 mol) 4-phenyl-1-(phenylmethyl)-1H-imidazole in 100 ml acetonitrile/10 ml DMF. After 18 hour, the dark yellow reaction was warmed at 70° C. for 7 hours. After cooling, 4.5 ml (0.0325 mol) triethylamine was added and the reaction stirred overnight. The reaction was quenched with 300 ml saturated NaHCO3 and extracted into ethyl acetate (3×150 ml). After drying and concentration, a tan oil was obtained. Flash chromatography (500 ml silica gel, EtOAc) gave 3.7 g recovered starting material and 2.26 g of the desired product (84% based on recovered starting material) mp 95°-96° C. (cyclohexane).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05147863 |
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| Quelldatensatz | uspto-grants-1992_09 |
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| ORD ID | ord-d7203e6f53a74c109ead9dccf259f21f |
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| Quellennotiz | uspto-grants-1992_09 |
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