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HRID 263824생성일: 2026년 10월 27일

Benzene, 1-bromo-3-iodo- → ((3-Bromophenyl)ethynyl)trimethylsilane

https://huagongshe.com/reaction/263824

반응식

참여 물질

역할이름HCID투입량
반응물Benzene, 1-bromo-3-iodo-HCID 11561—
반응물TrimethylsilylacetyleneHCID 66111—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매DiisopropylamineHCID 7912—
생성물((3-Bromophenyl)ethynyl)trimethylsilaneHCID 368332491%

반응 단계

To a solution of m-bromoiodobenzene (25.0 g. 881.1 mmol) in diisopropylamine (500 ml), there were added bis(triphenylphosphine)palladium dichloride (1.24 g. 1.80 mmol) and copper (I) iodide (1.24 g, 2.03 mmol). The solution was degassed via a rapid stream of argon, and trimethylsilylacetylene (9.51 g, 97.0 mmol) was added over a period of 15 min. The reaction mixture was stirred at room temperature until G.C. analysis indicated the disappearance of starting material (2 h). The reaction mixture was cooled to room temperature and filtered to remove salts. The filtrate was concentrated in vacuo, and the oily residue was taken up in dichloromethane. The solution was washed with an aqueous 5% HCl solution (2×200 ml), water (2×200 ml) and brine (1×200 ml). The combined organic layers were dried (MgSO4) and the solvent removed in vacuo yielding the crude product as a yellow oil. The liquid chromatographed from silica gel in pentane. Elution with pentane gave the product (1b) (20.59 g, 91%) as a clear liquid: bp 81°-82° C., 1H NMR (200 MHz, CDCl3) c 0.30 (s), 7.23(m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05645809
출처 데이터셋uspto-grants-1997_07
ORD IDord-f4c74cf4c1a64b56a5c4629dad152d89
출처 메모uspto-grants-1997_07