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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593982Generated: October 27, 2026

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

https://huagongshe.com/reaction/593982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant3-ChlorothiopheneHCID 87017—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
Product(3-Chlorothiophen-2-yl)trimethylsilaneHCID 19350967—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242961B2
Source datasetuspto-grants-2016_01
ORD IDord-75c103fe29a1409fbbc8ced8bf8f5e30
Source noteuspto-grants-2016_01