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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 963432생성일: 2026년 10월 25일

p-Bromoacetophenone → 1-(4-Ethynylphenyl)ethan-1-one

https://huagongshe.com/reaction/963432

반응식

참여 물질

역할이름HCID투입량
반응물p-BromoacetophenoneHCID 7466—
반응물TriethylamineHCID 8471—
반응물Potassium CarbonateHCID 11430—
반응물TrimethylsilylacetyleneHCID 66111—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
생성물1-(4-Ethynylphenyl)ethan-1-oneHCID 512362671%

반응 단계

2 g of 4-bromoacetophenone, 2.8 ml of ethynyltrimethylsilane, 140 mg of bis(triphenylphosphine)palladium dichloride, 3 ml of triethylamine and 14 mg of copper(I)iodide in 20 ml of N,N-dimethylformamide were stirred at 50° under argon for 2 hrs. After distillation of the solvent the residue was extracted once with 50 ml of ethyl acetate, once with 50 ml of 1N HCl and twice with 50 ml of water. The crude product was purified by silica gel chromatography in hexane/ethyl acetate 10:1 and distilled at 120°/0.1 Torr in a bulb-tube oven. 1.74 g (80%) were obtained as a colourless oil. This was dissolved in 17 ml of methanol, treated with 110 mg of potassium carbonate and stirred at room temperature for 1.5 hrs. After evaporation the product was extracted with 20 ml of ethyl acetate and 20 ml of water and then crystallized from 10 ml of hexane. 0.8 g (71%) of 1-(4-ethynyl-phenyl)-ethanone was obtained as white crystals. M.p. 71°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05763450
출처 데이터셋uspto-grants-1998_06
ORD IDord-0b11cb7be4414163baec91f68e5235e8
출처 메모uspto-grants-1998_06