This submission belongs to the session a. General Organic Synthesis of the event The 14th International Electronic Conference on Synthetic Organic Chemistry
Published date
21 Oct, 2010
Citation
Matilde Fondo, Jesús Sanmartín, Cristina Portela, Ana M. García-Deibe, Imine-tetrahydroquinazoline tautomerism in a tosilated Schiff base, in Proceedings of The 14th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2010, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-14-00426
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Imine-tetrahydroquinazoline tautomerism in a tosilated Schiff base
Matilde Fondo 1
Jesús Sanmartín 2
Cristina Portela 2
Ana M. García-Deibe 1
1. Departamento de Química Inorgánica, Facultade de Ciencias, Univ. de Santiago de Compostela, E-27002 Lugo, Spain
2. Departamento de Química Inorgánica, Facultade de Química, Universidade de Santiago de Compostela, E-15782 Santiago de Compostela, Spain
Abstract
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
Keywords
Imine-tetrahydroquinazoline
tautomerism
Schiff base
Double imidazolidine condensation in a polynucleating Schiff base
Synthesis and Characterization of Photomodulable Amphiphiles