We describe the catalytic amination of β-(hetero)arylethyl ethers with amines using the organic superbase -Bu-P4 to obtain β-(hetero)arylethylamines. The reaction has a broad substrate scope and allows the transformations of electron-deficient and electron-neutral β-(hetero)arylethyl ethers with various amines including pyrrole, -alkylaniline, diphenylamine, aniline, indole, and indoline derivatives. Mechanistic studies indicate a two-reaction pathway of MeOH elimination from the substrate to form a (hetero)arylalkene followed by the hydroamination of the alkene.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.orglett.9b02309 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!