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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711527Generated: November 1, 2026

3,5-Dibromopyridine → 3-Bromo-5-methoxypyridine

https://huagongshe.com/reaction/1711527

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-DibromopyridineHCID 69369—
ReactantSodium MethoxideHCID 10942334—
CatalystCopperHCID 23978—
SolventMethanolHCID 887—
Product3-Bromo-5-methoxypyridineHCID 81716359.5%

Reaction Conditions

Temperature150 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790757B2
Source datasetuspto-grants-2010_09
ORD IDord-a2e249ceeaa24fa59f3e1b45cc07ca4e
Source noteuspto-grants-2010_09