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HRID 477899作成日:2026年10月25日

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

https://huagongshe.com/reaction/477899

反応式

関与物質

役割名称HCID仕込み量
反応物TrimethylsilylacetyleneHCID 66111—
反応物2-Iodo-5-methylthiopheneHCID 140096—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418476HCID 178418476—
溶媒Diethyl EtherHCID 3283—
溶媒TriethylamineHCID 8471—
生成物(5-Methyl-2-thienylethynyl)trimethylsilaneHCID 1464357992.6%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04889867
出典データセットuspto-grants-1989_12
ORD IDord-bc788479251e400fa5ab1b1dc35ed022
出典メモuspto-grants-1989_12