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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 84178Erstellt: 23. Oktober 2026

Benzenesulfonyl chloride → 1H-Indole-5-carboxylic acid, 1-(phenylsulfonyl)-, methyl ester

https://huagongshe.com/de/reaction/84178

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenesulfonyl chlorideHCID 7369—
EduktPotassium HydroxideHCID 14797—
Eduktmethyl 1H-indole-5-carboxylateHCID 2737635—
LösungsmittelDichloromethaneHCID 6344—
Produkt1H-Indole-5-carboxylic acid, 1-(phenylsulfonyl)-, methyl esterHCID 57517433—

Reaktionsschritte

After a suspension of methyl indole-5-carboxylate (1) (0.30 g, 1.71 mmol), TB AHS (0.19 g, 0.26 mmol) and KOH (0.19 g, 3.42 mmol) in CH2Cl2 (15 mL) was stirred for 20 min, benzenesulfonyl chloride (0.32 ml, 2.57 mmol) was added. The reaction mixture was stirred at room temperature overnight before it was quenched with water and extracted with CH2Cl2 (20 mL×3). The combined organic layer was dried over anhydrous MgSO4 and concentrated under reduced pressure to give a yellow residue.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846748B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-109b10c8a30f45ad98f0915e1c6d9527
Quellennotizuspto-grants-2014_09