Реакция #2275668

ord-e1d4d7bf453541dc8fcc959b068e1d90

Уравнение реакции

Cc1ccc(S(=O)(=O)O)cc1
p-toluenesulfonic acid
O=Cc1ccc(C(=O)O)cc1
4-carboxybenzaldehyde
NS(=O)(=O)c1ccccc1
benzenesulfonamide
Cc1ccccc1
toluene
O=C(O)C1=CCC(=C=NS(=O)(=O)c2ccccc2)C=C1
4-{[(phenylsulfonyl)imino]methylidene}benzoic acid

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe mixture was then heated
  2. 2
    Другоеhad separated
  3. 3
    Фильтрацияthe precipitated solid was filtered off
  4. 4
    Другоеdried under vacuum

Методика

An equimolar mixture of 25.0 g (0.17 mol) 4-carboxybenzaldehyde and 26.7 g (0.17 mol) benzenesulfonamide was placed into toluene. 100 mg p-toluenesulfonic acid was added as a catalyst. The mixture was then heated under reflux on a water separator until the theoretically calculated quantity of water had separated. After cooling to room temperature, the precipitated solid was filtered off and dried under vacuum. Yield: 45.7 g (94.8%); 1H-NMR (400 MHz, DMSO-d6): δ [ppm]=7.59 (m, 2H); 7.78 (d, 1H); 8.02 (m, 2H); 8.12 (d, 2H); 8.18 (d, 2H); 9.30 (s, 1H); 13C-NMR (400 MHz, DMSO-d6): δ [ppm]=127.8; 129.7; 131.4; 134.1; 135.8; 136.0; 137.9; 166.5; 171.2; 192.9.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08323356B2uspto-grants-2012_12