Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064302Generated: October 30, 2026

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

https://huagongshe.com/reaction/2064302

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 numberUS08288420B2
Source datasetuspto-grants-2012_10
ORD IDord-ca54dee81d4d4af78b8a98279ec9ad44
Source noteuspto-grants-2012_10