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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983029Generated: October 30, 2026

Acetic Acid → HCID 22561914, compound

https://huagongshe.com/reaction/983029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthanolHCID 702—
ReactantPyridiniumtribromideHCID 21124087—
Reactant4-(3,4-Dimethoxyphenyl)-1H-indoleHCID 22561684—
CatalystZincHCID 23994—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
ProductHCID 22561914HCID 2256191465%

Reaction Steps

To the suspension of 4-(3,4-dimethoxy-phenyl)-1H-indole (14.7 g, 58 mmol) in t-BuOH: ethanol: acetic acid (367 mL: 217 mL: 113 mL) was added pyridinium tribromide (55.68 g, 174 mmol) portionwise. The mixture was stirred at room temperature for 3 hours, and then to the mixture was added more acetic acid (287 mL). Zinc dust (18.95 g, 290 mmol) was added to the reaction mixture portionwise. After stirring for one hour, water was added to the reaction. The 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 (6×), sat. NaHCO3 (2×), brine (3×), dried over Na2SO4, concentrated and triturated with ether to give 10.14 g (65%) of 4-(3,4-dimethoxy-phenyl)-1,3-dihydro-indol-2-one as an earth colored solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06861418B2
Source datasetuspto-grants-2005_03
ORD IDord-92d31f892f444d61b8be89c4eb00fc2e
Source noteuspto-grants-2005_03