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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715540Generated: October 31, 2026

N-bromobutanimide → 2-(Bromomethyl)-5-ethoxypyrazine

https://huagongshe.com/reaction/715540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Methyl-5-ethoxypyrazineHCID 105758—
SolventCarbon TetrachlorideHCID 5943—
SolventSodium BicarbonateHCID 516892—
Product2-(Bromomethyl)-5-ethoxypyrazineHCID 8671759732%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187464B2
Source datasetuspto-grants-2015_11
ORD IDord-390445fb987e49ddb77db1465298543e
Source noteuspto-grants-2015_11