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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 599495생성일: 2026년 10월 24일

Tetramethylene sulfoxide → 2-Chloro-5-[(1-oxidotetrahydrothien-2-yl)methyl]-pyridine

https://huagongshe.com/ko/reaction/599495

반응식

참여 물질

역할이름HCID투입량
반응물Tetramethylene sulfoxideHCID 1128—
반응물Trifluoroacetic acidHCID 6422—
반응물HexaneHCID 8058—
반응물2-Chloro-5-(chloromethyl)pyridineHCID 155479—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2-Chloro-5-[(1-oxidotetrahydrothien-2-yl)methyl]-pyridineHCID 5921522235%

반응 조건

온도-70 °C

반응 단계

Tetramethylene sulfoxide (6.5 g, 62 mmol) was dissolved in 30 mL anhydrous THF, stirred and cooled to −70° C. and then treated with 2.5 M n-BuLi in hexane (24 mL, 61 mmol) over a period of 10 min. The temperature was raised to −20 to −30° C. (Liquid N2/o-xylene bath) and the mixture was stirred for a further 30 min. The mixture was cooled to −70° C. and treated dropwise with a solution of 6-chloro-3-chloromethylpyridine in 15 mL THF. The reaction was stirred for 2 h at −70° C. and then treated dropwise with trifluoroacetic acid (8.0 g, 70 mmol). The mixture was warmed to room temperature, poured into 75 mL water and extracted with dichloromethane (2×50 mL). The combined organic extracts were washed with dilute sodium bicarbonate and saturated NaCl, dried over Na2SO4 and concentrated. The residue was chromatographed on silica gel with 5% methanol in dichloromethane to give 2.5 g of the desired sulfoxide as a brown oil in 35% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07897782B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-e811abdec18e474cb8af7e43b57acb20
출처 메모uspto-grants-2011_03