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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23412Erstellt: 25. Oktober 2026

1,1-Dichloroethane → 5-chloro-1H-indole-3-sulfonic acid

https://huagongshe.com/reaction/23412

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1-DichloroethaneHCID 6365—
EduktTrimethylsilyl chlorosulphateHCID 78059—
Edukt7-chloro-1H-indoleHCID 104644—
Produkt5-chloro-1H-indole-3-sulfonic acidHCID 22574052—

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

7-Chloroindole (1.51 g, 10 mmole) was dissolved in 2 ml dichloroethane and cooled under nitrogen to −10° C. in an ice-salt-acetone bath. Trimethylsilylchlorosulfonate (1.89 g, 1.6 ml, 10 mmole) was slowly added with stirring. Upon termination of the addition, the reaction was allowed to warm to room temperature and stirred for 30 min at this temperature. The dark red solution was evaporated to dryness and the solvent was replaced with 50 ml ethyl acetate. Methanol (5 ml) was added and the solvents were removed and the residue thoroughly dried to afford the crude 5-chloro-1H-indole-3-sulfonic acid as a red oil. Step 2 7-Chloro-1H-indole-3-sulfonic acid dimethylamide

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06852726B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-70c1fae9fcc645429cb95f1019463575
Quellennotizuspto-grants-2005_02