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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 983004Erstellt: 25. Oktober 2026

Water → 4-Phenylindolin-2-one

https://huagongshe.com/reaction/983004

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4-Phenyl-1H-indoleHCID 15806298—
EduktPyridiniumtribromideHCID 21124087—
KatalysatorZincHCID 23994—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelEthanolHCID 702—
Lösungsmitteltert-ButanolHCID 6386—
Produkt4-Phenylindolin-2-oneHCID 1304860167%

Reaktionsschritte

To the suspension of 4-phenyl-1H-indole (1.1 g, 5.7 mmol) in 2-methyl-2-propanol (33 mL), ethanol (22 mL) and acetic acid (11 mL) was added pyridinium tribromide (90% purity from Aldrich, 6.1 g, 17.1 mmol) portionwise over 10 minutes. The mixture was stirred at room temperature for 2 hours, and then to the mixture was added acetic acid (50 mL). After stirring at room temperature for one hour, water (0.5 mL) and zinc (3.7 g, 57 mmol) were added to the reaction mixture and stirring was continued for another hour. The unreacted zinc dust was filtered off and washed with methanol. The filtrate was concentrated and the syrupy residue was suspended in water (100 mL) for overnight. The solid product was filtered, washed repeatedly with water to remove the zinc salt and pyridine salt. After high vacuum dry, 800 mg (67%) of 4-phenyl-1,3-dihydro-indol-2-one as a light yellow solid was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06861418B2
Quelldatensatzuspto-grants-2005_03
ORD IDord-019143f702134c938a561e745cea973f
Quellennotizuspto-grants-2005_03