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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 983012Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/983012

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktPyridiniumtribromideHCID 21124087—
Edukt4-(4-Methoxyphenyl)-1H-indoleHCID 22561940—
KatalysatorZincHCID 23994—
Lösungsmittelt-BuOH ethanol aceticacidHCID 86587657—
Produkt4-(3-Methoxy-phenyl)-1,3-dihydro indol-2-oneHCID 2256180952%

Reaktionsbedingungen

Temperatur27 °C

Reaktionsschritte

To the suspension of 4-(4-methoxy-phenyl)-1H-indole (1.73 g, 7.75 mmol) in t-BuOH-ethanol-acetic acid (3:2:1) (93 mL) was added pyridinium tribromide (90% purity from Aldrich, 8.26 g, 23.24 mmol)) portionwise. The mixture was stirred at 27° C. for 3 hours, and then to the mixture was added acetic acid (38 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-methoxy-phenyl)-1,3-dihydro-indol-2-one (0.97 g, 52%) as a tan solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06861418B2
Quelldatensatzuspto-grants-2005_03
ORD IDord-afe4d2ed4cda473e8a4ad1fb38a39744
Quellennotizuspto-grants-2005_03