Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983030Generated: October 30, 2026

Acetic Acid → HCID 22561690, compound

https://huagongshe.com/reaction/983030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthanolHCID 702—
ReactantPyridiniumtribromideHCID 21124087—
ReactantHCID 22561717HCID 22561717—
CatalystZincHCID 23994—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
ProductHCID 22561690HCID 2256169032%

Reaction Steps

To the suspension of 2-[3-(1H-indol-4-yl)phenoxy)-ethanol (5.4 g, 21 mmol) in t-BuOH: ethanol: acetic acid (139.5 mL: 84 mL: 100.5 mL) was added pyridinium tribromide (21.21 g, 63 mmol) portionwise. The mixture was stirred at room temperature for 3 hours, and then to the mixture was added more acetic acid (90 mL) and water (3 mL). Zinc dust (21 g) was added to the reaction mixture portionwise. After stirring for one hour, 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 1N HCl (3×), water (1×), brine (2×), dried over Na2SO4, concentrated. The residue was recrystallized to give 1.82 g (32%) of 4-[3-(2-hydroxy-ethoxy)phenyl]-1,3-dihydro-indol-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06861418B2
Source datasetuspto-grants-2005_03
ORD IDord-2ed733a54fd549569fa7c7e5ae54a4c9
Source noteuspto-grants-2005_03