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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457544Generated: October 29, 2026

Methanol → 3-Bromo-5-methoxypyridine

https://huagongshe.com/reaction/457544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant3,5-DibromopyridineHCID 69369—
ReactantSodium MethoxideHCID 10942334—
SolventDimethylformamideHCID 6228—
Product3-Bromo-5-methoxypyridineHCID 81716393%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 3,5-dibromopyridine (134a, 20 g, 84.4 mmol) in DMF (200 mL) was stirred at RT under nitrogen atmosphere and then 21.3 mL of sodium methoxide (25% by wt. in methanol (92.8 mmol) was added slowly. The reaction mixture was stirred overnight at 70° C. under N2. The reaction was cooled to RT and quenched with water (200 mL) and extracted with Et2O (2×200 mL). The combined organic extracts was washed with brine, dried (MgSO4) and concentrated in vacuo. The crude 3-bromo-5-methoxypyridine (134b 14.8 g, 93% theory) afforded a colorless oil after purification by flash chromatography on silica gel (EtOAc:hexane 1:10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07189718B2
Source datasetuspto-grants-2007_03
ORD IDord-152fe4edc59341489631dd7f6fa4cb82
Source noteuspto-grants-2007_03