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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242417Generated: October 25, 2026

Water → 5-Bromo-4-chloro-2-methoxypyridine

https://huagongshe.com/reaction/242417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant4-Chloro-2-methoxypyridineHCID 22638510—
SolventDimethylformamideHCID 6228—
Product5-Bromo-4-chloro-2-methoxypyridineHCID 2313364980%

Reaction Steps

5.76 g (40.1 mmol) of 4-chloro-2-methoxypyridine was dissolved in 20 ml of dimethylformamide, and a dimethylformamide (20 ml) solution of 8.01 g of N-bromosuccinimide (98%, 44.1 mmol) was dropwise added over a period of 30 minutes. After stirring at room temperature for 2 days, an unreacted material was confirmed, and thus 2.85 g of N-bromosuccinimide (98%, 16 mmol) was further added, followed by stirring at room temperature further for 3 days. The reaction mixture was poured into 250 ml of water, followed by extraction with ethyl ether (100 ml each) three times. The organic layer was washed with water (100 ml), a sodium thiosulfate aqueous solution (100 ml) and then a saturated sodium chloride solution (100 ml), dried over magnesium sulfate and subjected to filtration, and the solvent was distilled off under reduced pressure. The obtained crude product was purified by silica gel chromatography to obtain 7.10 g (yield: 80%) of 5-bromo-4-chloro-2-methoxypyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653113B2
Source datasetuspto-grants-2014_02
ORD IDord-cacfd21f510247c488a1c47dd88d936e
Source noteuspto-grants-2014_02