Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508136Generated: October 30, 2026

p-Aminoacetophenone → 1-(4-Amino-3-bromo-phenyl)-ethanone

https://huagongshe.com/reaction/1508136

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-AminoacetophenoneHCID 7468—
ReactantN-bromobutanimideHCID 67184—
SolventAcetonitrileHCID 6342—
Product1-(4-Amino-3-bromo-phenyl)-ethanoneHCID 151528185%

Reaction Steps

To a solution of 4-aminoacetophenone (5.67 g, 0.0419 mol) in 30 mL of CH3CN at 0° C. was added N-bromosuccinimide (7.83 g, 0.0439 mol) in 20 mL of CH3CN dropwise. The reaction was allowed to warm to room temperature and concentrated in vacuo after stirring 16 h. The crude residue was dissolved in EtOAc (100 mL), washed with saturated aqueous NaHCO3 (1×100 mL), brine (1×100 mL) and dried (Na2SO4). The solvent was removed under vacuum to afford the title compound (7.62 g, 85%) as a yellow solid. Mass spectrum (ESI, m/z): Calcd. for C8H8BrNO, 213.9 (M+H). found 214.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221797B2
Source datasetuspto-grants-2015_12
ORD IDord-61db2ab273554d48ad38bae457ecc39e
Source noteuspto-grants-2015_12