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HRID 271729생성일: 2026년 10월 26일

Triethylamine → (4-Bromo-thiophen-2-ylethynyl)-trimethyl-silane

https://huagongshe.com/reaction/271729

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물TrimethylsilylacetyleneHCID 66111—
반응물Thiophene, 2,4-dibromo-HCID 2724560—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매TetrahydrofuranHCID 8028—
생성물(4-Bromo-thiophen-2-ylethynyl)-trimethyl-silaneHCID 67364285—

반응 조건

온도-78 °C

반응 단계

Under an argon atmosphere 0.37 g (1.94 mmol) CuI, 2.24 g (1.94 mmol) tetrakis-triphenylphosphane-palladium and 16.2 mL triethylamine are added to a solution of 10.0 g (38.85 mmol) 2,4-dibromothiophene in 300 mL THF, the reaction mixture is cooled to −78° C. and then at this temperature a solution of 5.6 mL (38.85 mmol) ethynyl-trimethyl-silane in 250 mL THF is slowly added dropwise. After the addition has ended the mixture is allowed to heat up slowly to RT and stirred overnight. The mixture is evaporated down i.vac., the residue is combined with water, extracted exhaustively with DCM and the combined organic phases are dried over MgSO4. After the desiccant and solvent have been eliminated the residue is triturated with PE, filtered to remove insoluble ingredients and the solvent is evaporated down. The residue is purified by chromatography (silica gel, PE).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07452911B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-c8b60b39523b4910834b0eeac7c0c3b7
출처 메모uspto-grants-2008_11