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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 227464Erstellt: 25. Oktober 2026

Sulfuric Acid → 5-Chloro-2-(ethoxycarbonyl)-1-(phenylsulfonyl)-1H-indole-3-sulfonic acid

https://huagongshe.com/reaction/227464

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktAcetic AnhydrideHCID 7918—
Eduktethyl 5-chloro-1-(phenylsulfonyl)-1H-indole-2-carboxylateHCID 22401489—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-Chloro-2-(ethoxycarbonyl)-1-(phenylsulfonyl)-1H-indole-3-sulfonic acidHCID 22401504—

Reaktionsschritte

To a solution of ethyl 5-chloro-1-(phenylsulfonyl)-1H-indole-2-carboxylate (5.56 g, 15.3 mmol) in 50 mL of dichloromethane at 0° C. was added acetic anhydride (7.23 mL, 76.6 mmol), followed by dropwise addition of concentrated sulfuric acid. The solution was warmed to room temperature, stirred for 3 hours, and partitioned between 0.5 L of EtOAc and 0.5 L of 3N HCl solution. The organic phase was washed with brine, dried with Na2SO4, filtered, and concentrated in vacuo. The product was reconcentrated from benzene in vacuo to give the titled product as a yellow solid. Proton NMR for the product was consistent with the titled compound of the formula C17H14ClNO7S2·.0.5 CH3CO2H. ESI+MS: 444.0 [M+H]+, 466.0 [M+Na]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07560546B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-12aa959e86ee487b84a223329d25a229
Quellennotizuspto-grants-2009_07