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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2772생성일: 2026년 10월 23일

Dichloromethane → 5-Pyridin-3-yl-thiophene-2-sulfonyl chloride

https://huagongshe.com/ko/reaction/2772

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Sulfuryl chlorideHCID 24648—
반응물3-(2-Thienyl)pyridineHCID 595145—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물5-Pyridin-3-yl-thiophene-2-sulfonyl chlorideHCID 1065897679.1%

반응 단계

To a solution of 3-thiophen-2-yl-pyridine (0.355 g, 2.20 mmol) in 15 mL of THF at -78° C. is added n-BuLi (1.44 mL of a 1.6M solution in hexanes, 2.31 mmol). After stirring for 15 min, SO2 gas is bubbled through the solution for 30 min. The solution is then allowed to warm to room temperature and stirred overnight. The solution is concentrated to dryness and the resulting solid is suspended in 20 mL of hexane. Sulfuryl chloride (0.185 mL, 2.31 mmol) is added and the reaction mixture is stirred for 30 min then a small amount of methylene chloride is added and the mixture is stirred for another 30 min. The mixture is then concentrated to dryness and diluted with ethyl acetate and washed with saturated NaHCO3 (aq), water and brine. The organic layer is dried over MgSO4, filtered and concentrated to give a brown solid as the title product (0.452 g, 1.74 mmol) which is used in the subsequent step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731315
출처 데이터셋uspto-grants-1998_03
ORD IDord-385105c7ada24b3c981f877c5e6c950f
출처 메모uspto-grants-1998_03