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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Bromo-5-(1-ethoxyethenyl)pyrazine | HCID 59166584 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Potassium Fluoride | HCID 522689 | — |
| Product | 2-Bromo-1-(5-bromopyrazin-2-yl)ethan-1-one | HCID 86690074 | 47.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09326973B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-e3aaaf9f95e84df5a3d9b3c756a2d559 |
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| Source note | uspto-grants-2016_05 |
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