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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 477899Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/477899

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilylacetyleneHCID 66111—
Edukt2-Iodo-5-methylthiopheneHCID 140096—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTriethylamineHCID 8471—
Produkt(5-Methyl-2-thienylethynyl)trimethylsilaneHCID 1464357992,6%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04889867
Quelldatensatzuspto-grants-1989_12
ORD IDord-bc788479251e400fa5ab1b1dc35ed022
Quellennotizuspto-grants-1989_12