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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 593982Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/593982

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktChlorotrimethylsilaneHCID 6397—
Edukt3-ChlorothiopheneHCID 87017—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt(3-Chlorothiophen-2-yl)trimethylsilaneHCID 19350967—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09242961B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-75c103fe29a1409fbbc8ced8bf8f5e30
Quellennotizuspto-grants-2016_01