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HRID 278818생성일: 2026년 10월 27일

Tetrahydrofuran → 2,6-Di-tert-butyl4-trimethylsilanylethynyl-phenol

https://huagongshe.com/reaction/278818

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물TriethylamineHCID 8471—
반응물TrimethylsilylacetyleneHCID 66111—
반응물4-Bromo-2,6-di-tert-butylphenolHCID 70829—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매HexaneHCID 8058—
생성물2,6-Di-tert-butyl4-trimethylsilanylethynyl-phenolHCID 22568924—

반응 단계

Following General Procedure D and using 4-bromo-2,6-di-t-butyl-phenol (1.43 g, 5 mmol), triethyl amine (15 mL), anhydrous tetrahydrofuran (15 mL), copper(I)iodide (0.06 g, 0.31 mmol), trimethylsilyl acetylene (4.9 g, 50 mmol) and dichlorobis(triphenylphosphine)palladium(II) (0.18 g, 0.26 mmol) followed by flash column chromatography over silica gel (230-400 mesh) using hexane as eluent, the title compound was obtained (1.35 g, 90%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06359135B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-8ff3afb9026d4ee78247be9304a27af1
출처 메모uspto-grants-2002_03