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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 430773Erstellt: 24. Oktober 2026

Benzyl Bromide → 4-(phenylmethoxy)-1H-indole

https://huagongshe.com/de/reaction/430773

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktPotassium HydroxideHCID 14797—
Edukt1H-indol-4-olHCID 75421—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(phenylmethoxy)-1H-indoleHCID 8846585%

Reaktionsschritte

Potassium hydroxide (0.42 g) was added to 4-hydroxyindole (1.00 g) in DMF (25 ml), and the solution was stirred at room temperature for 15 minutes. Benzyl bromide (1.00 ml) was added to the solution, and the solution was stirred at room temperature for 1.5 hours. Since the reaction was not completed, benzyl bromide (0.20 ml) was further added and the solution was stirred for 5 hours. After removing the solvent under reduced pressure, water (50 ml) was added to the residue and the resultant was extracted with ether (3×50 ml). The organic layers were washed with saturated brine, and dried over sodium sulfate. After removing solids by filtration, the solvent was removed under reduced pressure and the obtained crude product was purified by silica gel column chromatography to obtain the desired product (1.43 g, yield: 85%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06323235B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-ded0112ca83f4afa952d72e5c70ce665
Quellennotizuspto-grants-2001_11