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HRID 1750925Erstellt: 25. Oktober 2026
Phosphorus pentachloride → 1-(2,4-diisobutyldibenzo[b,d]furan-3-yl)-2-phenyl-4,5-dihydro-1H-imidazole
https://huagongshe.com/reaction/1750925
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phosphorus pentachloride | HCID 24819 | — |
| Edukt | N-(2-chloroethyl)benzamide | HCID 101439 | — |
| Edukt | 2,4-Diisobutyldibenzofuran-3-amine | HCID 58401063 | — |
| Lösungsmittel | M-Xylene | HCID 7929 | — |
| Produkt | 1-(2,4-diisobutyldibenzo[b,d]furan-3-yl)-2-phenyl-4,5-dihydro-1H-imidazole | HCID 58400929 | 77% |
Reaktionsschritte
N-(2-chloroethyl)benzamide (3.1 g, 16.88 mmol) was dissolved in 40 mL anhydrous m-xylene under nitrogen. Phosphorus pentachloride (5.27 g, 25.3 mmol) was then carefully added and the mixture heated to reflux under nitrogen for 2 h. The solution was allowed to cooled to room temperature and 2,4-diisobutyldibenzo[b,d]furan-3-amine (5.49 g, 18.57 mmol) was added. The reaction mixture was heated to reflux for 20 h. After cooling, the precipitate was filtered and the solid imidazoline product was collected and washed with toluene followed by hexanes. The resultant crude product was dissolved in methylene chloride and washed twice with 50% NaOH. The organic layer was dried over MgSO4, filtered and concentrated under reduced pressure to afford title product (5.5 g, 77%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09156870B2 |
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| Quelldatensatz | uspto-grants-2015_10 |
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| ORD ID | ord-a9b684a2ba3f4b76b6853098168e78de |
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| Quellennotiz | uspto-grants-2015_10 |
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