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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839605Generated: October 25, 2026

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

https://huagongshe.com/reaction/1839605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPyridiniumtribromideHCID 21124087—
Reactant4-(4-Chloro-phenyl)-1H-indoleHCID 22561747—
CatalystZincHCID 23994—
Solventt-BuOH ethanol aceticacidHCID 86587657—
Product4-(4-Chlorophenyl)-1,3-dihydro-indol-2-oneHCID 2256198994%

Reaction Conditions

Temperature27 °C

Reaction Steps

To the suspension of 4-(4-chloro-phenyl)-1H-indole (1.52 g, 6.68 mmol) in t-BuOH-ethanol-acetic acid (3:2:1) (81 mL) was added pyridinium tribromide (90% purity from Aldrich, 7.12 g, 20.0 mmol)) portionwise. The mixture was stirred at 27° C. for 3 hours, and then to the mixture was added acetic acid (30 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 suspended in water (500 mL) for 0.5 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 (1.54 g, 94%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677368B2
Source datasetuspto-grants-2004_01
ORD IDord-db13ae8ec8e74ef195ffb20f270bd421
Source noteuspto-grants-2004_01