摘要
The present paper describes a simple reduction of N-arylidene- and N-heteroarylideneamines from salicylaldehyde, thiophene-2-carboxaldehyde and N-methylindole-3-carboxaldehyde to the corresponding secondary amines by a simple method using sodium borohydride on neutral alumina under solvent-free conditions. The new products have been characterized by analytical and spectral data (IR, H-1 and C-13 NMR, MS). The mass spectra of N-substituted benzhydryl amines (alkyl amines) showed the molecular ion peak corresponding to M+ -2 and not M+ as shown by the N-substituted aromatic amines that has been explained by the possibility of formation of a more stable radical in the former type.
- 出版日期2014-12