戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 593982作成日:2026年10月27日

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

https://huagongshe.com/reaction/593982

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物ChlorotrimethylsilaneHCID 6397—
反応物3-ChlorothiopheneHCID 87017—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
溶媒Sodium chloride; waterHCID 57417360—
生成物(3-Chlorothiophen-2-yl)trimethylsilaneHCID 19350967—

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09242961B2
出典データセットuspto-grants-2016_01
ORD IDord-75c103fe29a1409fbbc8ced8bf8f5e30
出典メモuspto-grants-2016_01