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HRID 271729作成日:2026年10月25日

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

https://huagongshe.com/reaction/271729

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物TrimethylsilylacetyleneHCID 66111—
反応物Thiophene, 2,4-dibromo-HCID 2724560—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒TetrahydrofuranHCID 8028—
生成物(4-Bromo-thiophen-2-ylethynyl)-trimethyl-silaneHCID 67364285—

反応条件

温度-78 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07452911B2
出典データセットuspto-grants-2008_11
ORD IDord-c8b60b39523b4910834b0eeac7c0c3b7
出典メモuspto-grants-2008_11