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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983024Generated: October 31, 2026

Acetic Acid → HCID 22561683, compound

https://huagongshe.com/reaction/983024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantHCID 22561922HCID 22561922—
CatalystZincHCID 23994—
Solventtert-ButanolHCID 6386—
ProductHCID 22561683HCID 22561683—

Reaction Steps

To the suspension of {2-[3-(1H-indol-4-yl)-phenyl]-ethyl}-dimethyl-amine (600 mg, 2.2 mmol) in t-BuOH: ethanol: acetic acid (14.5 mL: 8.8 mL: 10.5 mL) was added pyridiniumn tribromide (2.3 g, 6.6 mmol) portionwise. The mixture was stirred at room temperature for 3 hours, and then to the mixture was added acetic acid (9.24 mL). Water (0.32 mL) and zinc dust (2.2 g, 61.2 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 and concentrated. The residue was dissolved in methanol (10 mL) and hydrogenated using 10% Pd-C for overnight. The reaction was filtered through celite and the filtrate was concentrated. The residue was purified on a silica gel column to give 4-[3-(2-dimethylamino-ethyl)-phenyl]-1,3-dihydro-indol-2-one

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06861418B2
Source datasetuspto-grants-2005_03
ORD IDord-4711df3c444142c5b628a26625687be3
Source noteuspto-grants-2005_03