Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 930926Erstellt: 25. Oktober 2026

Iodoethane → 3-Bromo-2-chloro-5-(ethylsulfonyl)pyridine

https://huagongshe.com/reaction/930926

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodoethaneHCID 6340—
EduktSodium SulfiteHCID 24437—
EduktSodium BicarbonateHCID 516892—
Edukt5-Bromo-6-chloropyridine-3-sulfonyl chlorideHCID 2793626—
LösungsmittelWaterHCID 962—
Produkt3-Bromo-2-chloro-5-(ethylsulfonyl)pyridineHCID 59326565—

Reaktionsbedingungen

Temperatur75 °C

Reaktionsschritte

Sodium sulfite (1.755 g, 13.92 mmol) and sodium bicarbonate (1.231 g, 14.65 mmol) were dissolved in water (37 mL) to give a colorless solution. The mixture was heated at 75° C. 3-Bromo-2-chloropyridine-5-sulfonyl chloride (2.132 g, 7.33 mmol) was added portionwise over 1 hour. The reaction mixture was stirred at 75° C. for 1 hour. The mixture was concentrated and N,N-dimethylformamide (13.88 mL) was added. Sodium bicarbonate (1.231 g, 14.65 mmol) and iodoethane (0.589 mL, 7.33 mmol) were added. The resulting mixture was heated to 75° C. for 2 hours and then cooled to ambient temperature. The mixture was partitioned between ethyl acetate and water. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated. The residue was purified by flash chromatography (silica gel, 0-100% ethyl acetate/heptane) to provide the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09296741B2
Quelldatensatzuspto-grants-2016_03
ORD IDord-84952ea5e3604f048e593a31dd7ee4df
Quellennotizuspto-grants-2016_03