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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-Bromo-2-methoxy-5-methylpyridine | HCID 21952757 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Bromo-5-bromomethyl-2-methoxy-pyridine | HCID 58539510 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08049015B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-b498dc09ecbe4ac1b5fba8be030db570 |
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| Source note | uspto-grants-2011_11 |
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