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HRID 227804생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/227804

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물ChlorotrimethylsilaneHCID 6397—
반응물3-ChlorothiopheneHCID 87017—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
용매Sodium chloride; waterHCID 57417360—
생성물(3-Chlorothiophen-2-yl)trimethylsilaneHCID 19350967—

반응 조건

온도0 °C

반응 단계

The title compound was prepared according to the procedure described in WO9412505. To a solution of 3-chlorothiophene (7.00 g, 59.0 mmol) in 60 mL anhydrous THF under nitrogen was added n-butyllithium, 2.5 M in hexanes (23.6 ml, 59.0 mmol) dropwise from a plastic syringe over 15 min. The reaction became cloudy with a white ppt. The reaction was allowed to stir for 40 min, at which point trimethylsilyl chloride (8.24 ml, 64.9 mmol) was added dropwise via syringe over 5 min. The mixture was allowed to stir for 10 min, and was then warmed to 0° C. for 10 min, and 7 mL water and 35 mL brine were added. The mixture was diluted with EtOAc, and the layers separated. The aqueous layer was extracted once with EtOAc. The combined organics were dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to give (3-chlorothiophen-2-yl)trimethylsilane as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560551B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-cdbe6f7d20f3471ba6e8c4781bd2a99e
출처 메모uspto-grants-2009_07