HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489766Generated: October 30, 2026
3,5-Dibromopyridine → 3-Bromo-5-methoxypyridine
https://huagongshe.com/reaction/489766
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,5-Dibromopyridine | HCID 69369 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Bromo-5-methoxypyridine | HCID 817163 | 59.5% |
Reaction Steps
A mixture of 3,5-dibromopyridine (20.00 g, 84.42 mmol), sodium methoxide (11.40 g, 211.06 mmol), and copper powder (1 g, 5% by weight of 3,5-dibromopyridine) in dry methanol was heated in a sealed glass tube at 150° C. for 14 h. The reaction mixture was cooled to ambient temperature and extracted with diethyl ether (4×200 mL). The combined ether extracts were dried over sodium sulfate, filtered, and concentrated by rotary evaporation. The crude product was purified by column chromatography over aluminum oxide, eluting with ethyl acetate-hexane (1:9, v/v). Selected fractions were combined and concentrated by rotary evaporation, producing 9.40 g (59.5%) of a colorless oil, which tended to crystallize upon cooling.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06979695B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-a21eb3be94fe4902abc1ea810956c04a |
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| Source note | uspto-grants-2005_12 |
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