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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1159763Erstellt: 27. Oktober 2026

o-Toluenesulfonyl chloride → 4-Bromo-1-(2-methyl-benzenesulfonyl)-1H-indole

https://huagongshe.com/reaction/1159763

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukto-Toluenesulfonyl chlorideHCID 8623—
EduktSodium HydroxideHCID 14798—
Edukt4-BromoindoleHCID 676494—
KatalysatorTetrabutylammonium hydrogen sulfateHCID 94433—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Bromo-1-(2-methyl-benzenesulfonyl)-1H-indoleHCID 2201533454%

Reaktionsschritte

Aq. 2.5 M NaOH (5 mL) was added to a stirring mixture of 4-bromo-1H-indole (1000 mg, 5.3 mmol), 2-methylbenzenesulfonyl chloride (1100 mg, 5.6 mmol) and tetrabutylammonium hydrogen sulfate (173 mg, 0.5 mmol) in DCM (10 mL). The reaction mixture was stirred at ambient temperature overnight. The mixture was diluted with DCM and water and the layers were separated. DCM was washed with water 2 times, dried (MgSO2) and concentrated to give 1.6 g of crude material that was purified using flash chromatography (SiO2, eluent EtOAc:hexane 9:1) giving the title product (1 g, 54%). MS (ESI+) for C15H12BrNO2S m/z 350 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07812017B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-3218029980604fa5ab77b0b0aeb011a5
Quellennotizuspto-grants-2010_10