HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 56237Erstellt: 24. Oktober 2026
Diiodomethane → 3-((6-nitro-1H-indol-1-yl)methoxy)benzonitrile
https://huagongshe.com/de/reaction/56237
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diiodomethane | HCID 6346 | — |
| Edukt | 3-Cyanophenol | HCID 13394 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 6-Nitro-1H-indole | HCID 78502 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 3-((6-nitro-1H-indol-1-yl)methoxy)benzonitrile | HCID 90030447 | 51% |
Reaktionsschritte
To a mixture of NaH (3.0 g, 75.0 mmol, 60%) in DMF (20 mL) were added a solution of 6-nitro-1H-indole (4.86 g, 30.0 mmol) in DMF (10 mL) and a solution of 3-hydroxybenzonitrile (3.57 g, 30.0 mmol) in DMF (10 mL) at 0° C. and the mixture was stirred at rt for 2 h. To the reaction mixture was added a solution of diiodomethane (7.5 mL, 90.0 mmol) in DMF (10 mL) slowly without light and the mixture was stirred at rt for 20 h. The mixture was then quenched with water and filtered. The filtrate was extracted with DCM (30 mL×6) and the combined organic layers were washed with brine (50 mL×3), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:1) to give the title compound as a yellow solid (4.47 g, 51%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09434695B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-4ac7af751afe4a0c8814018ded4486d1 |
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| Quellennotiz | uspto-grants-2016_09 |
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