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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471157Generated: October 31, 2026

N-bromobutanimide → 2-Bromo-1-(6-bromoquinoxalin-2-yl)ethanone

https://huagongshe.com/reaction/1471157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant6-Bromo-2-(1-ethoxyvinyl)quinoxalineHCID 58498763—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-1-(6-bromoquinoxalin-2-yl)ethanoneHCID 5849865659%

Reaction Steps

NBS (55.1 mg, 0.310 mmol) was added to a solution of 6-bromo-2-(1-ethoxyvinyl)quinoxaline (72 mg, 0.26 mmol) in THF (2 mL) and water (0.500 mL) and the mixture was stirred at rt for 2 h. The reaction was diluted with MeOH and purified by prep HPLC (H2O-MeOH with 10 mM NH4OAc buffer) to yield 2-bromo-1-(6-bromoquinoxalin-2-yl)ethanone (50 mg, 0.15 mmol, 59% yield) as white solid. LC-MS retention time 2.40 min; m/z 329 [M+H]+. (Column PHENOMENEX® Luna 3.0×50 mm S10. Solvent A=90% water:10% methanol:0.1% TFA. Solvent B=10% water:90% methanol:0.1% TFA. Flow Rate=4 mL/min. Start % B=0. Final % B=100. Gradient Time=3 min. Wavelength=220).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006455B2
Source datasetuspto-grants-2015_04
ORD IDord-34315cc8024c4be1b4daea9a1aa9a8b4
Source noteuspto-grants-2015_04