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Abstract
A series of N-(p-X-phenyl)-N′-(p-toluenesulfonyl)1,2-ethylenediamines compounds, TsN(H)CH2CH2N(H)PhX, were synthesized by the uncatalyzed ring opening reaction of N-tosylaziridine with p-X-aniline derivatives in pure water at 50°C. No solvolysis product was observed and the only side product was that of a subsequent ring opening reactions of N-tosylaziridine with the product anilines leading to substituted diethylenetriamines, XPhN(CH2CH2NTs)2.
Published Version
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