Chemistry of chromotropic acid. ¹H and ¹³C NMR spectroscopy of chromotropic acid and its derivatives

Abstract

. J. Chem. 69, 1207 (1991).The 'H and I3C NMR spectra of chromotropic acid (CTA) (4,5-dihydroxy-2,7-naphthalenedisulphonic acid) have been unambiguously assigned. Proton NOED spectra were used to show the proximity of both H-3 and H-6 and the hydroxyl groups. Two-dimensional 'H-'~c NMR correlation spectra of CTA, of its corresponding diacetoxy derivative, and of 3-bromo-and 3,6-dibromo-CTA support the assignments. A regioselective deuterium exchange reaction of the C-3 and C-6 protons of CTA with deuterium oxide was observed during the NMR experiments. This latter finding is strongly indicative of the mode of formation, and of the nature of the chromogen formed in the reaction of CTA with formaldehyde in the well-known CTA-formaldehyde analytical reaction.