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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2270969Erstellt: 24. Oktober 2026

Acetic Anhydride → 3-Acetyl-1-benzenesulfonylindole-5-carboxylic acid methyl ester

https://huagongshe.com/de/reaction/2270969

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
EduktAluminum(III) ChlorideHCID 6451240—
Edukt1H-Indole-5-carboxylic acid, 1-(phenylsulfonyl)-, methyl esterHCID 57517433—
Lösungsmittel1,1-DichloroethaneHCID 6365—
Produkt3-Acetyl-1-benzenesulfonylindole-5-carboxylic acid methyl esterHCID 6989028096%

Reaktionsschritte

To a suspension of 10.7 g (80 mmol) of aluminum chloride in dichloroethane (80 ml) was added dropwise 4.83 g (40 mmol) of acetic anhydride. After stirring for 15 min, to the mixture was added dropwise 6.31 g (20 mmol) of the above-mentioned 1-benzenesulfonylindole-5-carboxylic acid methyl ester in dichloroethane (60 ml). After stirring for 2 hours at room temperature, to the mixture were added 5.33 g (40 mmol) of aluminum chloride and 2.04 g (20 mmol) of acetic anhydride. After stirring for 30 min, the mixture was poured into ice-water, extracted with ethyl acetate. The extract was washed twice with water, aqueous sodium bicarbonate and dried, and then concentrated. The obtained crystal was washed with isopropyl ether to give 6.82 g of 3-acetyl-1-benzenesulfonylindole-5-carboxylic acid methyl ester. Yield: 96%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06333323B1
Quelldatensatzuspto-grants-2001_12
ORD IDord-7988fd239167492c82cfcab229980e81
Quellennotizuspto-grants-2001_12