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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839603Generated: November 3, 2026

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

https://huagongshe.com/reaction/1839603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPyridiniumtribromideHCID 21124087—
Reactant4-(4-fluorophenyl)-1H-indoleHCID 22561686—
CatalystZincHCID 23994—
Solventt-BuOH ethanol aceticacidHCID 86587657—
Product4-(4-Fluoro-phenyl)-1,3-dihydro-indol-2-oneHCID 2256185298%

Reaction Conditions

Temperature27 °C

Reaction Steps

To the suspension of 4-(4-fluoro-phenyl)-1H-indole (2.28 g, 10.79 mmol) in t-BuOH-ethanol-acetic acid (3:2:1) (147 mL) was added pyridinium tribromide (90% purity from Aldrich, 11.51 g, 32.38 mmol)) portionwise. The mixture was stirred at 27° C. for 3 hours, and then to the mixture was added acetic acid (108 mL). Zinc dust (10.52 g, 162 mmol) was added to the reaction mixture portionwise, 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 suspended in water for 4 hour. The solid product was precipitated out, filtered, and washed repeatedly with water to remove the zinc salt and pyridine salt. After high vacuum dry, a pure product (2.40 g, 98%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677368B2
Source datasetuspto-grants-2004_01
ORD IDord-76556d42b5f64c71a6321a76741582a9
Source noteuspto-grants-2004_01