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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839625Generated: November 2, 2026

Acetic Acid → HCID 22561961, compound

https://huagongshe.com/reaction/1839625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthanolHCID 702—
ReactantPyridiniumtribromideHCID 21124087—
Reactant3-(1H-Indol-4-yl)benzoic acidHCID 22561954—
CatalystZincHCID 23994—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
ProductHCID 22561961HCID 2256196177%

Reaction Steps

To the suspension of 3-(1H-indol-4-yl)-benzoic acid (7.58 g, 33 mmol) in t-BuOH:ethanol:acetic acid (150 mL:100 mL:50 mL) was added pyridinium tribromide (31.66 g, 99 mmol) portionwise. The mixture was stirred at room temperature for 2 hours, and then to the mixture was added with acetic acid (150 mL). Water (4 mL) and Zinc dust (13.07 g, 200 mmol) was added to the reaction mixture portionwise and stirring was continued at room temperature for 2 hours. The solvent was removed under reduced pressure. The oily residue was suspended in 1N HCl (400 mL) and stirred at room temperature overnight. The precipitate solid was collected by filtration, purified by recrystallization from ethyl acetate to give (6.4 g, 77%) of 3-(2-oxo-2,3-dihydro-1H-indol-4-yl)-benzoic acid as a pinkish white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677368B2
Source datasetuspto-grants-2004_01
ORD IDord-cdc89896ba7b4cb9879b8b70fea634d9
Source noteuspto-grants-2004_01