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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50033Erstellt: 25. Oktober 2026

Dichloromethane → Ethyl 5-chloro-3-(3,5-dimeihylphenylthio)-6-fluoroindole-2-carboxylate

https://huagongshe.com/reaction/50033

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktBoron trifluoride etherateHCID 8000—
EduktN-(3,5-Dimethylphenylthio)succinimideHCID 11053620—
EduktEthyl 5-chloro-6-fluoro-1H-indole-2-carboxylateHCID 11413806—
LösungsmittelChloroformHCID 6212—
LösungsmittelSodium chloride; waterHCID 57417360—
ProduktEthyl 5-chloro-3-(3,5-dimeihylphenylthio)-6-fluoroindole-2-carboxylateHCID 21301066102,4%

Reaktionsschritte

Boron trifluoride ethyl etherate (0.135 g, 0.12 mL, 0.001 mol) was added to a mixture of ethyl 5-chloro-6-fluoroindole-2-carboxylate (0.75 g, 0.0031 mol), N-(3,5-dimethylphenylthio)-succinimide (0.78 g, 0.0033 mol) and anhydrous dichloromethane (20 mL) under dry argon atmosphere. After stirring at room temperature for 2 hours was added boron trifluoride ethyl etherate (0.27 g, 0.24 mL, 0.002 mol) and then reaction was heated at 45° C. for 2 hours. After cooling reaction was diluted chloroform and brine while shaking. Organic layer was separated, washed with saturated solution of sodium hydrogen carbonate, then with brine and dried. The solvent was evaporated to give 1.2 g (100%) of satisfactory pure title compound, mp 170-173° C. (from ethanol).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06710068B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-72582ea7baff4f51bacbd7e698208507
Quellennotizuspto-grants-2004_03