HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 62172Erstellt: 24. Oktober 2026
Potassium Hydroxide → 3,6-dibromo-9-((oxiran-2-yl)methyl)-9H-carbazole
https://huagongshe.com/de/reaction/62172
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Epibromohydrin | HCID 18430 | — |
| Edukt | 3,6-Dibromocarbazole | HCID 274874 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 3,6-dibromo-9-((oxiran-2-yl)methyl)-9H-carbazole | HCID 2775473 | 66,3% |
Reaktionsschritte
Following a literature procedure (Asso, V.; Ghilardi, E.; Bertini, S.; Digiacomo, M.; Granchi, C.; Minutolo, F.; Rapposelli, S.; Bortolato, A.; Moro, S. Macchia, M. ChemMedChem, 2008, 3, 1530-1534) powdered KOH (0.103 g, 1.85 mmol) was added to a solution of 3,6-dibromocarbazole (0.500 g, 1.54 mmol) in DMF (1.5 mL) at ambient temperature and stirred for 30 min until dissolved. Epibromohydrin (0.32 mL, 3.8 mmol) was added via syringe and the reaction was stirred at room temperature overnight. Upon completion, the solution was partitioned between EtOAc and H2O. The aqueous layer was washed 3× with EtOAc, and the combined organics were washed with saturated aqueous NaCl, dried over Na2SO4, filtered, and concentrated in vacuo. The crude residue was recrystallized from EtOAc/Hexane to afford the desired product (389 mg, 66%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09446042B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-32a255d7c63a48e4a5b9df1859013124 |
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| Quellennotiz | uspto-grants-2016_09 |
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