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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1868421Erstellt: 25. Oktober 2026

1-Benzenesulfonyl-3-phenylindole → 3-Phenylindole

https://huagongshe.com/reaction/1868421

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Benzenesulfonyl-3-phenylindoleHCID 11110394—
LösungsmittelMethanolHCID 887—
LösungsmittelPotassium HydroxideHCID 14797—
Produkt3-PhenylindoleHCID 9650234%

Reaktionsschritte

A mixture of 245 mg (0.73 mmol) of 1-benzenesulfonyl-3-phenyl-1H-indole in 10 mL of methanol and 5 mL of 2 N aqueous KOH was warmed at reflux for 2 hours. The mixture was then cooled and concentrated in vacuo and diluted with water and extracted with ethyl acetate. The combined organic layers were washed with two 10 mL portions of 2 N aqueous KOH solution, 10 mL of brine, three 10 mL portions of saturated aqueous ammonium chloride solution, and 10 mL of brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The crude material was triturated with hexanes afford 48 mg (33%) of 3-phenyl-1H-indole.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07635711B2
Quelldatensatzuspto-grants-2009_12
ORD IDord-ee16478e78714573a4446dcd0b50fc67
Quellennotizuspto-grants-2009_12