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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6380생성일: 2026년 10월 23일

1-Butyne → 2-(But-1-yn-1-yl)-benzenesulfonamide

https://huagongshe.com/ko/reaction/6380

반응식

참여 물질

역할이름HCID투입량
반응물1-ButyneHCID 7846—
반응물TriethylamineHCID 8471—
반응물2-Iodobenzene-1-sulfonamideHCID 2824892—
촉매Copper iodideHCID 83717—
촉매HCID 178418476HCID 178418476—
용매DimethylformamideHCID 6228—
생성물2-(But-1-yn-1-yl)-benzenesulfonamideHCID 19793588—

반응 단계

0.1 g of bis(triphenylphosphine)palladium(II) chloride, 0.05 g of copper iodide and 18.5 ml of triethylamine are added to a solution of 5 g of 2-iodobenzenesulfonamide in 70 ml of N,N-dimethylformamide. At room temperature, argon and 1-butyne are slowly introduced. After 18 hours the thin-layer chromatogram no longer shows any 2-iodobenzenesulfonamide. The dimethylformamide is evaporated off at 0.1 torr and 40°, and the residue is chromatographed on 300 g of silica gel (Merck ST 60, 40-63 μm). Methylene chloride is used as eluant. In that manner, after concentration of the product-containing fractions at 15 torr and 40°, white pulverulent 2-(but-1-yn-1-yl)-benzenesulfonamide is obtained: 1H-NMR (300 MHz, CDCl3): 8.0 (d, d, 1H); 7.35 (d, d, 1H); 7.29 (d, t, 1H); 7.23 (d, t, 1H); 5.13 (s, 2H); 2.32 (q, 2H); 1.18 (t, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05248693
출처 데이터셋uspto-grants-1993_09
ORD IDord-c34b896f8df643aab6bb098bc5e91b2c
출처 메모uspto-grants-1993_09