HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715540Generated: October 31, 2026
N-bromobutanimide → 2-(Bromomethyl)-5-ethoxypyrazine
https://huagongshe.com/reaction/715540
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Methyl-5-ethoxypyrazine | HCID 105758 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 2-(Bromomethyl)-5-ethoxypyrazine | HCID 86717597 | 32% |
Reaction Steps
A mixture of 2-ethoxy-5-methylpyrazine (0.86 g, 6.22 mmol), NBS (1.440 g, 8.09 mmol), and diphenylperoxyanhydride (0.151 g, 0.622 mmol) in carbon tetrachloride (20 mL) was heated to 80° C. overnight. Cooled to RT, diluted with saturated NaHCO3, and extracted with ethyl acetate (3×). The combined organic extracts were washed with saturated NaCl (2×), dried over Na2SO4, filtered, and concentrated. The residue was purified via ISCO (40 g silica, 40 mL/min, 0-30% EtOAc/Hexanes over 25 min) to afford 2-(bromomethyl)-5-ethoxypyrazine (430 mg, 32%). MS (m/z) 217.0 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187464B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-390445fb987e49ddb77db1465298543e |
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| Source note | uspto-grants-2015_11 |
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