HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 51298Erstellt: 24. Oktober 2026
Phenethyl bromide → 1-Phenethyl-1H-imidazole-4-carbaldehyde
https://huagongshe.com/de/reaction/51298
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Phenethyl bromide | HCID 7666 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 1H-Imidazole-4-carbaldehyde | HCID 76428 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-Phenethyl-1H-imidazole-4-carbaldehyde | HCID 22289872 | — |
Reaktionsschritte
Imidazole-4-carboxaldehyde (6.73 g, 70 mmol) was added portionwise to a suspension of sodium hydride (1.68 g, 60% dispersion in mineral oil, 70 mmol) in tetrahydrofuran (280 ml), and the mixture was then stirred at room temperature for 30 minutes. (2-Bromoethyl)benzene (9.56 ml, 70 mmol) was added, and the mixture was stirred at room temperature for 72 hours. The mixture was evaporated under reduced pressure and the residue was partitioned between water (300 ml) and dichloromethane (500 ml), and the layers were separated. The organic phase was dried (MgSO4) and evaporated under reduced pressure. The crude product was pre-adsorbed onto silica gel, and purified by column chromatography on silica gel using an elution gradient of ethyl acetate:pentane (50:50 to 100:0) to afford the title compound, 1.44 g. 1H-NMR (CDCl3, 400 MHz) δ: 3.16 (t, 2H), 4.23 (t, 2H), 7.02 (d, 2H), 7.28 (m, 3H), 7.36 (s, 1H), 7.50 (s, 1H), 9.83 (s, 1H). LRMS: m/z (ES+) 223 [MNa+].
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06713496B2 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-31441750fe72498fa9d8520b043eb1a1 |
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| Quellennotiz | uspto-grants-2004_03 |
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