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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 503914Erstellt: 26. Oktober 2026

Benzenesulfonyl chloride → 5-Fluoro-1-(phenylsulfonyl)-1H-indole

https://huagongshe.com/reaction/503914

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenesulfonyl chlorideHCID 7369—
Edukt5-FluoroindoleHCID 67861—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-Fluoro-1-(phenylsulfonyl)-1H-indoleHCID 1128885874%

Reaktionsschritte

KHMDS (0.5 M in toluene, 23 mL, 11.65 mmol) was added at 0° C. to a solution of 5-fluoroindole (1.5 g, 11.09 mmol) in DMF (23 mL). After stirring for 10 minutes, benzenesulfonyl chloride (1.55 mL, 12.209 mmol) was added. The ice-bath was removed and the mixture was stirred at room temperature for 4 hours. A saturated solution of NH4Cl was added to the reaction, and the resulting mixture was extracted with EtOAc. The combined organic extracts were washed with water and brine; dried over Na2SO4, filtered and evaporated under reduced pressure. The residue was recrystallized from toluene to afford 2.26 g (74% yield) of 1-benzenesulfonyl-5-fluoro-1H-indole as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07776910B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-fdc0db041e3c4731bbd8402309b37211
Quellennotizuspto-grants-2010_08