A study of some reactions of the intermediate isolated from the NN-dimethylaniline–tetracyanoethylene reaction
Abstract
It was previously suggested that the intermediate isolated from the NN-dimethylaniline–tetracyanoethylene reaction was zwitterionic. Synthetic and spectroscopic studies on this intermediate reported here indicate that a neutral substituted ethane structure is the correct one. The compounds formed by hydrolysis of the intermediate by acid and by base are described.
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