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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755015Generated: November 2, 2026

Water → HCID 66818770, compound

https://huagongshe.com/reaction/1755015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant4-BromoindoleHCID 676494—
Reactant2-Chloroethylamine hydrochlorideHCID 9793737—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventAcetonitrileHCID 6342—
ProductHCID 66818770HCID 6681877039%

Reaction Steps

Tetrabutylammonium hydrogen sulfate (41.0 mg, 0.121 mmol) and sodium hydroxide (210 mg, 5.25 mmol) were added to a solution of 4-bromo-1H-indole (0.30 ml, 2.39 mmol) in acetonitrile (0.80 mL), and the mixture was stirred at room temperature for 20 minutes. Subsequently, 2-chloroethylamine hydrochloride (334 mg, 2.88 mmol) was added and the mixture was heated with stirring at 100° C. for seven hours. After cooling, water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was sequentially washed with water and saturated brine and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (dichloromethane-methanol) to give 2-(4-bromo-indol-1-yl)-ethylamine (222 mg, 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169254B2
Source datasetuspto-grants-2015_10
ORD IDord-fab6e8c5118e45e4a854b2f40e76bcdc
Source noteuspto-grants-2015_10