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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476681Generated: November 1, 2026

Water → 2-(Trimethylsilylethynyl)thiophene

https://huagongshe.com/reaction/1476681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylamineHCID 7912—
Reactant2-IodothiopheneHCID 18921—
ReactantTrimethylsilylacetyleneHCID 66111—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
Product2-(Trimethylsilylethynyl)thiopheneHCID 59687069,747.898%

Reaction Steps

A mixture of 2-iodothiophene (500 mg, 2.38 mmol), Pd(PPh3)2Cl2 (52.95 mg, 0.0754 mmol), CuI (28.1 mg, 0.14756 mmol) and diisopropylamine (0.62 ml, 4.4744 mmol) in THF (4 ml) was degassed thoroughly with argon, and trimethylsilyl acetylene (0.453 ml, 3.284 mmol) was added at room temperature. After stirring the reaction mixture for 16 hours at room temperature, it was poured into water and extracted with dichloromethane. The combined organic layers were washed with brine and dried over anhydrous sodium sulfate, and the solvent was evaporated. The crude material was purified by column chromatography (100-200 mesh silica gel) using hexane as eluent to yield 300 mg of trimethyl(thiophen-2-ylethynyl)silane (300 mg, 1.66 mol, yield 70.02%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09402397B2
Source datasetuspto-grants-2016_08
ORD IDord-8d2b3040dc3046d9bf1746b0a962ed1e
Source noteuspto-grants-2016_08