Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406750Generated: October 31, 2026

Methanol → 3-Bromo-2-methoxy-5-nitropyridine

https://huagongshe.com/reaction/2406750

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant3-Bromo-2-chloro-5-nitropyridineHCID 230889—
ReactantSodium MethoxideHCID 10942334—
SolventWaterHCID 962—
Product3-Bromo-2-methoxy-5-nitropyridineHCID 21584451—

Reaction Steps

Sodium methoxide (28% methanol solution) (2 ml) was added to a methanol (2 ml) solution containing 3-bromo-2-chloro-5-nitropyridine (100 mg), followed by stirring at room temperature for 1 hour. Water was added to the reaction solution, followed by extraction with ethyl acetate. The resultant was washed with saturated saline and dried over anhydrous sodium sulfate, the solvent was distilled away under reduced pressure, and a yellow solid of 3-bromo-2-methoxy-5-nitropyridine (96 mg) was thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809371B2
Source datasetuspto-grants-2014_08
ORD IDord-49e0d9e9b6ca4d3d8c36e4611290405b
Source noteuspto-grants-2014_08