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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 243767Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/243767

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktN-bromobutanimideHCID 67184—
Edukt4-Chloro-2-methoxypyridineHCID 22638510—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-Bromo-4-chloro-2-methoxypyridineHCID 2313364979,6%

Reaktionsschritte

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: 30%) of 5-bromo-4-chloro-2-methoxypyridine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653277B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-01cac08b2fee45af83b656b9d30351b5
Quellennotizuspto-grants-2014_02