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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2284310Erstellt: 27. Oktober 2026

Benzenesulfonyl chloride → 1-benzenesulfonyl-3-bromo-6-nitro-1H-indole

https://huagongshe.com/reaction/2284310

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenesulfonyl chlorideHCID 7369—
EduktSodium hydrideHCID 24758—
Edukt3-Bromo-6-nitro-1H-indoleHCID 14707934—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-benzenesulfonyl-3-bromo-6-nitro-1H-indoleHCID 5744219676,5%

Reaktionsschritte

Sodium hydride (461 mg, 11.5 mmol) was slowly added to a solution of 3-bromo-6-nitro-1H-indole (2.32 g, 9.61 mmol) in tetrahydrofuran (10.0 mL). After stirring for 5 min, benzenesulfonyl chloride (1.47 mL, 11.5 mmol) was added dropwise over 10 min. The reaction was stirred an additional 1.5 h before quenching with 5.0 mL of methanol, followed by 10.0 mL water and 20.0 mL methylene chloride. The precipitate was filtered off and washed with an excess of methylene chloride and methanol to give a crème-colored powder for 3-bromo-6-nitro-1-(phenylsulfonyl)-1H-indole (2.80 g, 7.35 mmol, 76%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09144557B2
Quelldatensatzuspto-grants-2015_09
ORD IDord-61e947e1665143c7be2c4f5506605dfa
Quellennotizuspto-grants-2015_09