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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554649Generated: October 28, 2026

Azobisisobutyronitrile → 3-Bromo-5-bromomethyl-2-methoxy-pyridine

https://huagongshe.com/reaction/554649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant3-Bromo-2-methoxy-5-methylpyridineHCID 21952757—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product3-Bromo-5-bromomethyl-2-methoxy-pyridineHCID 58539510—

Reaction Conditions

Temperature80 °C

Reaction Steps

3-Bromo-2-methoxy-5-methyl-pyridine (4.0 g, 19.8 mmol), N-bromosuccinimide (4.45 g, 23.8 mmol), and azobisisobutyronitrile (0.163 g, 0.99 mmol) were combined in benzene (40 mL) and stirred overnight at 80° C. The reaction was stirred for another 24 hours at 80° C., and then additional N-bromosuccinimide (1.8 g, 10.1 mmol), and azobisisobutyronitrile (catalytic) were added. After stirring for another 2 hours at 80° C., the mixture was diluted with H2O and extracted with CH2Cl2. The residue was purified by silica gel chromatography to give 3-bromo-5-bromomethyl-2-methoxy-pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08049015B2
Source datasetuspto-grants-2011_11
ORD IDord-b498dc09ecbe4ac1b5fba8be030db570
Source noteuspto-grants-2011_11