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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 633553생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/633553

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참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물Sodium SulfiteHCID 24437—
반응물Sodium BicarbonateHCID 516892—
반응물5-Bromo-6-chloropyridine-3-sulfonyl chlorideHCID 2793626—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물3-Bromo-2-chloro-5-(ethylsulfonyl)pyridineHCID 5932656553.7%

반응 조건

온도75 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09321764B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-f7fb6e2e606b416c8e83f761f428c6e8
출처 메모uspto-grants-2016_04