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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232391Generated: October 25, 2026

Trimethylsilylacetylene → (5-Methyl-2-thienylethynyl)trimethylsilane

https://huagongshe.com/reaction/2232391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant2-Iodo-5-methylthiopheneHCID 140096—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDiethyl EtherHCID 3283—
SolventTriethylamineHCID 8471—
Product(5-Methyl-2-thienylethynyl)trimethylsilaneHCID 1464357992.6%

Reaction Steps

Under a dry nitrogen atmosphere 3.0 grams (0.031 mole) of trimethylsilylacetylene was added to a stirred mixture of 5.5 grams (0.025 mole) of 2-iodo-5-methylthiophene in 50 ml of triethylamine. To this mixture was added approximately 0.05 gram of dichlorobis(triphenylphosphine)palladium (II) and approximately 0.05 gram of copper (I) iodide. The resultant mixture was stirred at room temperature for approximately 18 hours. The triethylamine was removed from the mixture by evaporation under reduced pressure leaving a residue. This residue was dissolved in diethyl ether and the resultant solution was washed in succession with an aqueous, 10% ammonium chloride solution, water, and an aqueous, saturated sodium chloride solution. The washed organic solution was dried over anhydrous sodium sulfate and was filtered. The filtrate was evaporated under reduced pressure leaving a residue. This residue was purified by column chromatography on silica gel, eluting with n-hexane, to yield 4.5 grams of 1-trimethylsilyl-2-(5-methylthien-2-yl)ethyne as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04788207
Source datasetuspto-grants-1988_11
ORD IDord-665f763b6cd64fbdabbccb506c1f9b96
Source noteuspto-grants-1988_11