Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 983014Erstellt: 25. Oktober 2026

Acetic Acid → 4-(3-Trifluoromethyl-phenyl)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/983014

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktPyridiniumtribromideHCID 21124087—
Edukt4-(3-Trifluoromethyl-phenyl)-1H-indoleHCID 22561674—
KatalysatorZincHCID 23994—
Lösungsmittelt-BuOH ethanol aceticacidHCID 86587657—
Produkt4-(3-Trifluoromethyl-phenyl)-1,3-dihydro-indol-2-oneHCID 2256190558%

Reaktionsbedingungen

Temperatur27 °C

Reaktionsschritte

To the suspension of 4-(3-trifluoromethyl-phenyl)1H-indole (3.37 g, 12.90 mmol) in t-BuOH-ethanol-acetic acid (3:2:1) (155 mL) was added pyridinium tribromide (12.38 g, 38.70 mmol)) portionwise. The mixture was stirred at 27° C. for 3 hours, and then to the mixture was added acetic acid (63 mL). Zinc dust was added to the reaction mixture portionwise until the color changed from deep red to light yellow, and the reaction mixture was stirred at room temperature for one hour. The unreacted zinc dust was filtered off and washed with ethanol. The filtrate was concentrated, and the syrupy residue was dissolved in ethyl acetate, which was washed with water, 0.5 N HCl, sat. NaHCO3 and brine, and dried over Na2SO4. After filtration and evaporation, the crude product was triturated with diethyl ether to provide product 4-(3-trifluoromethyl-phenyl)-1,3-dihydro-indol-2-one (2.07 g, 58%) as a tan solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06861418B2
Quelldatensatzuspto-grants-2005_03
ORD IDord-9ab1bec94b2c411d98cfe53e53edfd7d
Quellennotizuspto-grants-2005_03