Abstract
A new stereoelectronic theory for the cleavage of the tetrahedral intermediate (hemiorthoamide) in the hydrolysis of amides is presented. In this new theory, the precise conformation of the tetrahedral intermediate controls the nature of the hydrolysis products. It is postulated that the breakdown of the tetrahedral intermediate depends upon the orientation of the lone pair orbitals of the heteroatoms. Specific cleavage of a carbon–oxygen or a carbon–nitrogen bond in any conformer is allowed only if the other heteroatoms (oxygen and nitrogen) each have an orbital oriented antiperiplanar to the leaving O-alkyl or N-alkyl group. Experimentally, a study of the basic hydrolysis of a variety of N,N-dialkylated imidate salts having either a syn or an anti conformation demonstrates clearly that there is a stereoelectronic control in the cleavage of the hemiorthoamide.
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