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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 265646생성일: 2026년 10월 25일

Chlorotrimethylsilane → (3-Chlorothiophen-2-yl)trimethylsilane

https://huagongshe.com/reaction/265646

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물3-ChlorothiopheneHCID 87017—
반응물Lithium ChlorideHCID 433294—
반응물Acetone cardiceHCID 18522661—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
용매Sodium chloride; waterHCID 57417360—
생성물(3-Chlorothiophen-2-yl)trimethylsilaneHCID 19350967—

반응 조건

온도0 °C

반응 단계

To 3-chlorothiophene (5.0 g, 42.16 mmol), dissolved in 50 mL of tetrahydrofuran stirring at -72° C. (acetone/dry ice bath), was added 16.8 ml of 2.5M hexane solution of n-butyllithium over a 15 minute period. The reaction temperature was maintained below -70° C. during the addition. Soon after complete addition of the n-butyllithium a white precipitate formed. After 40 minutes of stirring below -70° C., 5.88 mL of chlorotrimethylsilane was slowly added over a 5 minute period. After addition the solution momentarily became clear before turning cloudy again by the formation of lithium chloride by-product. After 10 minutes the reaction solution was warmed to 0° C. At 0° C. 5 mL of water followed by 25 mL of brine was added to quench the reaction. The aqueous solution was then extracted with ethyl acetate (2×30 mL). The organic extract was dried (Na2SO4), filtered and evaporated to 8.0 g of title compound as a clear oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05648502
출처 데이터셋uspto-grants-1997_07
ORD IDord-a7c399d1b5c245b098442ddf9d2319c0
출처 메모uspto-grants-1997_07