Imine-tetrahydroquinazoline tautomerism in a tosilated Schiff base

  1. García-Deibe, Ana 1
  2. Fondo, Matilde 1
  3. Sanmartín, Jesús 1
  4. Portela, Cristina 2
  1. 1 Departamento de Química Inorgánica, Facultade de Ciencias, Univ. de Santiago de Compostela, E-27002 Lugo, Spain
  2. 2 Departamento de Química Inorgánica, Facultade de Química, Universidade de Santiago de Compostela, E-15782 Santiago de Compostela, Spain
Actas:
Proceedings of The 14th International Electronic Conference on Synthetic Organic Chemistry

Ano de publicación: 2010

Tipo: Achega congreso

DOI: 10.3390/ECSOC-14-00426 GOOGLE SCHOLAR lock_openAcceso aberto editor

Resumo

Condensation of the selectively tosilated N-(2-aminobenzyl)-4-methylbenzenesulfonamide with 2-hydroxybenzaldehyde gives rise to (E)-N-(2-(2- hydroxybenzylideneamino)benzyl)-4-methylbenzenesulfonamide in the solid state, as the crystal structure determined shows, and which in solution shows equilibrium between the acyclic imine and 2-(3-tosyl-1,2,3,4-tetrahydroquinazolin-2-yl)phenol