Scope and limitations of a 1H NMR method for the prediction of substituted phenols pKa values in water, CH3CN, DMF, DMSO and i-PrOH

Abstract Simple empirical correlations were proposed between phenol p K a in various solvents (H 2 O, DMF, CH 3 CN, DMSO, and i -PrOH) and their chemical shifts δ OH measured in DMSO- d 6 . The following method permits to predict p K a values for most phenols in the studied solvents with a good accuracy when intramolecular interactions (hydrogen bonds, steric hindrance, and tautomeric resonance) can be neglected. To illustrate the scope of the method we applied it to nine complex monoprotic phenols for which Hammett substituent constants σ − were not compiled. The results obtained in water were in good agreement with the results obtained from ACD/p K a software and allowed to extend the calculation to their σ − Hammett substituent constants and p K a values in other solvents.