Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 57321Erstellt: 24. Oktober 2026

Cfc 113 → 4-chloro-5-fluoro-1H-indole-3-carboxylic acid

https://huagongshe.com/de/reaction/57321

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCfc 113HCID 6428—
EduktTetrahydrofuranHCID 8028—
Edukt4-MethylcatecholHCID 9958—
Edukt2,2,6,6-TetramethylpiperidineHCID 13035—
EduktPentamethyldiethylenetriamineHCID 18196—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
Produkt4-chloro-5-fluoro-1H-indole-3-carboxylic acidHCID 11864471773,8%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

2,2,6,6-Tetramethylpiperidine (1.06 g, 7.5 mmol), N,N′,N″,N″-pentamethyldiethylene triamine (3.46 g, 20 mmol) and compound 1 (1.45 g, 5.0 mmol) were added consecutively to a solution of n-BuLi (2.5 M in hexanes, 8 mL, 20 mmol) in THF (20 mL) and hexanes (6 mL) at −78° C. After stirring for 4 h at −78° C., the mixture was treated with 1,1,2-trichloro-1,2,2-trifluoroethane (1.18 g, 6.0 mmol) before it was warmed to 25° C. Water was added to the mixture. The organic phase was washed with brine, dried with sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by SiO2 column chromatography (PE) to provide title compound (1.2 g, 73.8%) as a colorless liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434724B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-62f0612a44624501baa69ff92d0919ac
Quellennotizuspto-grants-2016_09