The reaction of N-acetylglycine p-nitrophenyl ester with the anion of
an active methylene compound proceeds to give N-acetyl-3-butanoyltetra
mic acid. The influence of the N-acetyl group on the equilibrium betwe
en different 'internal' and 'external' tautomeric forms of N-acetyl-3-
butanoyltetramic acid was investigated by H-1 and C-13 NMR spectroscop
y. The structure of this compound was confirmed by an X-ray crystal st
ructure determination.