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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 477899생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물TrimethylsilylacetyleneHCID 66111—
반응물2-Iodo-5-methylthiopheneHCID 140096—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매Diethyl EtherHCID 3283—
용매TriethylamineHCID 8471—
생성물(5-Methyl-2-thienylethynyl)trimethylsilaneHCID 1464357992.6%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04889867
출처 데이터셋uspto-grants-1989_12
ORD IDord-bc788479251e400fa5ab1b1dc35ed022
출처 메모uspto-grants-1989_12