Abstract
The Chemistry of Amino Oximes, XIV Synthesis and Reaction of 2‐[α‐(E)‐(Hydroxyimino)benzyl]‐3‐imidazoline 3‐Oxides2‐Benzoyl‐4‐phenyl‐1‐(p‐tolyl)‐3‐imidazolin 3‐oxide (3b) has been prepared by cyclocondensation of α‐(p‐toluidino)acetophenone oxime (1a) with phenylglyoxal and transferred into 2‐[α‐(E)‐(hydroxyimino)benzyl]‐4‐phenyl‐1‐(p‐tolyl)‐3‐imidazoliune 3‐oxide (5a). 5a is identical with the product prepared by oxidation of 1a, with FeCl3.
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