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Theoretical Study on Amines: aniline, N-methylaniline, p-methylaniline and pmethyl-N-methylaniline
(2024) Caglieri, Silvana; Servetti, Gustavo Iván; Picco, Eduardo
The acetylation of amines is one of the most frequently used transformations in organic synthesis as it provides an efficient and inexpensive means for protecting amino groups in a multistep synthetic process. Geometric parameters of reactants: aniline,N-methylaniline,p-methylaniline1 and p-methyl-N-methylaniline were performed in the gas phase using the DFT/B3LYP density functional quantum mechanical method and was adopted the 3-21+G* basis set. Enthalpies of formation were determined using the AM1 method. The table lists the energies, lengths and angles values obtained. Steric effects caused by the additional methyl group might be responsible of an increase of the energy of N-methylaniline compared to aniline and an increase of the energy of p-methyl-N-methylaniline compared to p-methylaniline.