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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912258Generated: October 25, 2026

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

https://huagongshe.com/reaction/1912258

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 numberUS08609150B2
Source datasetuspto-grants-2013_12
ORD IDord-db4238b9ee3845f3b1493141df350e97
Source noteuspto-grants-2013_12