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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 551037Erstellt: 25. Oktober 2026

Benzenesulfonyl chloride → 4-Bromo-1-(phenylsulfonyl)-1H-indole

https://huagongshe.com/reaction/551037

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenesulfonyl chlorideHCID 7369—
EduktSodium hydrideHCID 24758—
Edukt4-BromoindoleHCID 676494—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-Bromo-1-(phenylsulfonyl)-1H-indoleHCID 22015311—

Reaktionsschritte

To a solution of 4-bromoindole (1.00 g, 5.10 mmol) in DMF (50 mL) at ambient temperature was added sodium hydride (220 mg of a 60% dispersion in mineral oil, 5.50 mmol). The reaction mixture was stirred for 5 min, then benzenesulfonyl chloride (901 mg, 5.10 mmol) was added and stirring was continued for 15 min. The reaction was quenched with saturated aqueous NaHCO3 (50 mL) and extracted with CHCl3 (2×75 mL). The combined organic extracts were dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—100:0 to 90:10, to give the title compound. MS: m/z=336 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07947677B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-c25a0b5ed9ed48e4afd66e9ad4ada2c4
Quellennotizuspto-grants-2011_05