Issue 10, 1970

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.

Article information

Article type
Paper

J. Chem. Soc. C, 1970, 1390-1394

A study of some reactions of the intermediate isolated from the NN-dimethylaniline–tetracyanoethylene reaction

P. G. Farrell and R. K. Wojtowski, J. Chem. Soc. C, 1970, 1390 DOI: 10.1039/J39700001390

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