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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1159752Erstellt: 24. Oktober 2026

4-Toluenesulfonyl chloride → 4-Bromo-1-(toluene-4-sulfonyl)-1H-indole

https://huagongshe.com/de/reaction/1159752

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Toluenesulfonyl chlorideHCID 7397—
EduktSodium HydroxideHCID 14798—
Edukt4-BromoindoleHCID 676494—
KatalysatorTetrabutylammonium hydrogen sulfateHCID 94433—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Bromo-1-(toluene-4-sulfonyl)-1H-indoleHCID 56286994%

Reaktionsschritte

4-Bromoindole (1.24 g, 6.3 mmol), p-toluenesulfonyl chloride (1.32 g, 6.9 mmol) and tetrabutyl-ammonium hydrogen sulfate (42 mg, 0.1 mmol) was dissolved in DCM (50 mL). NaOH 2.5 M aq (6 mL, 15 mmol) was added and the mixture was stirred vigorously for 1 h. Diluted with water and DCM, collected the DCM phase and washed it twice with water, dried and concentrated to give the product as white crystalline material (2.07 g, 5.9 mmol). Yield 94%. MS (ESI+) for C15H12BrNO2S m/z 352 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07812017B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-19adf0d4a9a74c9b8e6b5311acd2efe8
Quellennotizuspto-grants-2010_10