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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 633553Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/633553

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodoethaneHCID 6340—
EduktSodium SulfiteHCID 24437—
EduktSodium BicarbonateHCID 516892—
Edukt5-Bromo-6-chloropyridine-3-sulfonyl chlorideHCID 2793626—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-Bromo-2-chloro-5-(ethylsulfonyl)pyridineHCID 5932656553,7%

Reaktionsbedingungen

Temperatur75 °C

Reaktionsschritte

Sodium sulfite (4.94 g, 39.2 mmol) and sodium bicarbonate (3.46 g, 41.2 mmol) in water (100 mL) were heated to 75° C. 3-bromo-2-chloropyridine-5-sulfonyl chloride (6.00 g, 20.6 mmol) was added portionwise over 1 hour. The reaction mixture was stirred at 75° C. for 1 hour after complete addition. The mixture was concentrated under vacuum. N,N-Dimethylformamide (37.5 mL), sodium bicarbonate (3.46 g, 41.2 mmol) and iodoethane (1.658 mL, 20.62 mmol) were added. The resulting mixture was heated to 75° C. for 2 hours then cooled to room 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 reaction mixture was purified by flash chromatography (silica gel, 100% heptane to 100% ethyl acetate) to provide the title compound (3.15 g, 53% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09321764B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-f7fb6e2e606b416c8e83f761f428c6e8
Quellennotizuspto-grants-2016_04