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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiiodomethaneHCID 6346—
Edukt3-CyanophenolHCID 13394—
EduktSodium hydrideHCID 24758—
Edukt6-Nitro-1H-indoleHCID 78502—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-((6-nitro-1H-indol-1-yl)methoxy)benzonitrileHCID 9003044751%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434695B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-4ac7af751afe4a0c8814018ded4486d1
Quellennotizuspto-grants-2016_09