Abstract

2-Hydroxymethyl-pyridine with phenacyl bromide gives 3-hydroxy-3-phenyl-pyrido[2,1-c][1,4]dihydrooxazinium bromide ( 1). Its structure in crystal was determined by X-ray diffraction and confirmed by FTIR spectra and B3LYP calculations. In DMSO and D 2O solutions, this compound exists in equilibrium mixtures with N-phenacyl-2-hydroxymethyl-pyridinium bromide ( 2). The equilibrium mixture was proved by FTIR, 1H, 13C and 15N NMR spectra. Correlations between the experimental 1H and 13C NMR chemical shifts for 1 and 2 and GIAO/B3LYP/6-31G(d,p) calculated magnetic isotropic shielding tensors ( σ), δ exp= a+ bσ cal, are reported. A good linear relationship between the experimental and calculated data was obtained only for carbons.

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