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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8113Erstellt: 23. Oktober 2026

Sodium hydride → 5,7-difluoro-1H-indole

https://huagongshe.com/de/reaction/8113

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktEthyl acetate hexaneHCID 21226206—
Eduktethyl N-{2,4-difluoro-6-[2-(trimethylsilyl)ethynyl]phenyl}carbamateHCID 22014809—
LösungsmittelEthanolHCID 702—
ProduktSodium ethoxideHCID 2723922—
Produkt5,7-difluoro-1H-indoleHCID 277873078,4%

Reaktionsschritte

Fresh sodium ethoxide is prepared by carefully adding NaH (16 g of 60% oil dispersion, 400 mmol) to 550 mL of ethanol under N2. 2-(Trimethylsilylethynyl)-4,6-difluoro-N-carbethoxyaniline (28 g, 100 mmol) in 150 mL of ethanol is added and reaction is stirred at room temperature approximately 45 minutes, while monitoring by TLC (20% ethyl acetate/hexane, UV) until all the starting material is consumed. The mixture is heated to reflux and monitored by TLC until the intermediate material is consumed (approx. 1 hour). Reaction is cooled to room temperature, concentrated, diethylether is added, washed with H2O, brine, dried (Na2SO4), filtered, concentrated, and is purified by flash chromatography (SiO2, ethyl acetate/hexane gradient) to yield 12 g of 5,7-difluoro-indole (78%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087635B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-a9d09bb02bf34689b618636a056c80b1
Quellennotizuspto-grants-2006_08