반응 #6476

ord-c34b896f8df643aab6bb098bc5e91b2c

반응 방정식

NS(=O)(=O)c1ccccc1I
2-iodobenzenesulfonamide
CCN(CC)CC
triethylamine
NS(=O)(=O)c1ccccc1I
2-iodobenzenesulfonamide
C#CCC
1-butyne
CCC#Cc1ccccc1S(N)(=O)=O
2-(but-1-yn-1-yl)-benzenesulfonamide

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The dimethylformamide is evaporated off at 0.1 torr and 40°
  2. 2
    기타the residue is chromatographed on 300 g of silica gel (Merck ST 60, 40-63 μm)

실험 절차

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

DOI: 10.6084/m9.figshare.5104873.v1특허: US05248693uspto-grants-1993_09