| Literature DB >> 16092836 |
Masahiro Mizuno1, Mitsuhisa Yamano.
Abstract
A novel one-pot synthesis of anilines from phenols was developed. Using this methodology, anilines are produced in good yield (86%) by a reaction of phenols with 2-bromo-2-methylpropionamide and NaOH in DMA via Smiles rearrangement. Phenols, which are substituted electron-withdrawing groups, are more reactive for Smiles rearrangement. Thiophenols are also converted to anilines. The process is a convenient, safe, and inexpensive method for large-scale preparation of anilines. [reaction: see text]Entities:
Year: 2005 PMID: 16092836 DOI: 10.1021/ol051080k
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005