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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520350Generated: October 30, 2026

N-bromobutanimide → 2-Bromo-1-(5-bromopyrazin-2-yl)ethan-1-one

https://huagongshe.com/reaction/520350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Bromo-5-(1-ethoxyethenyl)pyrazineHCID 59166584—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventPotassium FluorideHCID 522689—
Product2-Bromo-1-(5-bromopyrazin-2-yl)ethan-1-oneHCID 8669007447.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-bromo-5-(1-ethoxyvinyl)pyrazine (0.65 g, 2.84 mmol) in THF and water was added NBS (0.505 g, 2.84 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 1 hr, then diluted with EtOAc and aq. KF. The two phase mixture was stirred for 20 min at rt before being filtered through diatomaceous earth (Celite®). The filtrate was washed with sat. NaHCO3, sat. NaCl, dried over anhydrous Na2SO4, concentrated. The crude product was purified by silica gel chromatography (0-100% EtOAc in hexane) to yield 2-bromo-1-(5-bromopyrazin-2-yl)ethanone (0.38 g) as a yellow oil. LC/MS (Cond. N-1): [M+H]+ 280.91, RT=2.945 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09326973B2
Source datasetuspto-grants-2016_05
ORD IDord-e3aaaf9f95e84df5a3d9b3c756a2d559
Source noteuspto-grants-2016_05