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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 855236Erstellt: 24. Oktober 2026

Carbon Dioxide → 5-chloro-1H-indole-7-carboxylic acid

https://huagongshe.com/de/reaction/855236

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
EduktWaterHCID 962—
Edukt7-bromo-5-chloro-1H-indoleHCID 24729504—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
Produkt5-chloro-1H-indole-7-carboxylic acidHCID 6686856372%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

1.15 g (5 mmol) of 7-bromo-5-chloro-1H-indole were dissolved in 30 ml THF. At a temperature of −75° C. under argon 9.4 ml (15 mmol) of a 1.6 M n-butyl lithium solution in hexane were added dropwise. After complete addition the reaction mixture was stirred at 5° C. for 30 min, cooled to −75° C. and 10 g dry ice was added. The reaction mixture was warmed to rt and stirred for 15 min. It was poured onto 100 ml of water and extracted twice with EtOAc. The aqueous layer was acidified with 1N aqueous HCl solution and extracted twice with DCM. The combined organic layers were dried over sodium sulfate, filtered and the solvent was evaporated. The residue was treated with hexane and stirred for 10 min. The precipitate was filtered, washed with hexane and dried to yield 700 mg (72%) of 5-chloro-1H-indole-7-carboxylic acid as a white solid. MS (ISP) 194.0 (M−H)−.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07259183B2
Quelldatensatzuspto-grants-2007_08
ORD IDord-97b659aed26e4d91af804825204b3d7b
Quellennotizuspto-grants-2007_08