NMR characterization of hydrate and aldehyde forms of imidazole-2-carboxaldehyde and derivatives

JUAN MANUEL LÁZARO MARTÍNEZ; PABLO NICOLÁS ROMASANTA; ANA KARINA CHATTAH; GRACIELA YOLANDA BULDAIN

JOURNAL OF ORGANIC CHEMISTRY

AMER CHEMICAL SOC

Lugar: Washington DC; Año: 2010 vol. 75 p. 3208 - 3213

0022-3263

The existence and stability of the aldehyde-hydrate form of imidazole-2-carboxaldehyde (4) were studied using FTIR together with solution- and solid-state NMR experiments. The results allowed us to conclude that the hydrate form was stable and precipitated at pH = 8.0, and that the aldehyde form was isolated at pH = 6.5 and 9.5. Moreover, the presence of the aldehyde-hydrate form was studied through NMR experiments in D2O at both alkaline and acidic pH. In addition, the tautomeric forms of the 2-substituted imidazole compounds were also analyzed to investigate the influence of the hybridization on the carbon adjacent to the imidazole ring, by 13C NMR in DMSO-d6, acetone-d6 and CDCl3. The presence of the syn- and anti-isomers of oxime 8 obtained from 4 were characterized by solid-state NMR and variable temperature NMR experiments in acetone-d6.