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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839632Generated: October 30, 2026

Acetic Acid → HCID 22561985, compound

https://huagongshe.com/reaction/1839632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthanolHCID 702—
ReactantPyridiniumtribromideHCID 21124087—
ReactantHCID 22561694HCID 22561694—
CatalystZincHCID 23994—
Solventtert-ButanolHCID 6386—
ProductHCID 22561985HCID 2256198576%

Reaction Steps

To the suspension of 4-(2-chloro-phenyl)-1H-indole (2.4 g, 10.6 mmol) in t-BuOH:ethanol:acetic acid (67 mL:40 mL:21 mL) was added pyridinium tribromide (10.5 g, 32 mmol) portionwise. The mixture was stirred at room temperature for 3 hours, and then to the mixture was added acetic acid (52 mL). Zinc dust (3.5 g, 53 mmol) was added to the reaction mixture portionwise. After stirring for one hour, any unreacted zinc was filtered off and most of the solvent was removed under reduced pressure. The residue was diluted with ethyl acetate, washed with water (3×), sat. NaHCO3, brine, dried over Na2SO4, concentrated and triturated with ether to give 1.96 g (76%) of 4-(2-chloro-phenyl)-1,3-dihydro-indol-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677368B2
Source datasetuspto-grants-2004_01
ORD IDord-a98e01a6566248aabf02e5ee6e412ea2
Source noteuspto-grants-2004_01