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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 248494Erstellt: 25. Oktober 2026

Benzenesulfonyl chloride → 1H-Indole, 3-acetyl-1-(phenylsulfonyl)-

https://huagongshe.com/reaction/248494

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenesulfonyl chlorideHCID 7369—
Edukt3-AcetylindoleHCID 12802—
EduktPotassium HydroxideHCID 14797—
EduktAmmonium ChlorideHCID 25517—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
Produkt1H-Indole, 3-acetyl-1-(phenylsulfonyl)-HCID 848535—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 41.39 g of 3-acetyl indole in 300 ml of dimethyl sulfoxide at 0° C. was added a solution of 18.6 g of potassium hydroxide in 20 ml of water. This mixture was stirred at 0° C. for 2 hours, then 47.6 ml of benzenesulfonyl chloride was added dropwise over 40 minutes. The mixture was stirred for an additional 30 mInutes, then poured into aqueous ammonium chloride and extracted several times with ether. The ether extracts were combined, washed with water, dried and evaporated, giving 59.8 g of 3-acetyl-N-phenylsulfonyl indole.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05210193
Quelldatensatzuspto-grants-1993_05
ORD IDord-3dcfc7d0edb84b4c8073d9f8123bacf1
Quellennotizuspto-grants-1993_05