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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 245239Erstellt: 24. Oktober 2026

5-Bromoisatin → 6-Bromo-3-methyl-2-[4-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid

https://huagongshe.com/de/reaction/245239

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-BromoisatinHCID 6889—
EduktPotassium HydroxideHCID 14797—
Eduktp-TrifluoromethylpropiophenoneHCID 136554—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt6-Bromo-3-methyl-2-[4-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acidHCID 6738362098%

Reaktionsschritte

A solution of potassium hydroxide (13.08 g, 233 mmol) in water (25.2 mL) was added slowly to a solution of 5-bromo-1H-indole-2,3-dione (9.76 g, 38.9 mmol) in ethanol (63.1 mL). 1-[4-(trifluoromethyl)phenyl]-1-propanone (8.64 g, 42.7 mmol) was added and the mixture was heated to reflux for 1 h. The reaction mixture was concentrated to remove the solvent, the residue was dissolved in water, and the mixture was washed three times with Et2O. The aqueous mixture was chilled, and concentrated HCl was added until the solution was pH 3. The solid was collected by filtration, washed with water, and dried under reduced pressure in a water bath at 100° C. The product was obtained as a light brown powder (15.6 g, 98%). This material was used without further purification. MS (m/z) 412.0 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658636B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-cf262dca2b0949e48e17846215830107
Quellennotizuspto-grants-2014_02