## Abstract The reaction of metallic sodium with phenyl, ethyl and benzyl phenyliminobenzoates has been investigated in an inert solvent. The main products are benzil‐dianil in case of the phenyl derivative, and benzanilide in case of the ethyl and benzyl derivatives. A free radical mechanism is po
Action du sodium sur les phénylimino-éthers. II. Condensation de quelques dérivés o- et p-substitués du phénylimino-benzoate de phényle
✍ Scribed by Roland Jaunin; Gabriel Séchaud
- Publisher
- John Wiley and Sons
- Year
- 1956
- Tongue
- German
- Weight
- 402 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
Phenyl phenglimino‐o‐ and p‐toluates (II and III resp.) and phenyl phenylimino‐o‐methoxybenzoate (IV) react readily with metallic sodium in ethyl ether to produce mainly substituted benzildianils. Under the same conditions, phenyl phenyliniino‐p‐methoxybenzoate (V) fails to react appreciably, but yields in boiling n‐butyl ether a complex mix‐ ture which can be partially hydrolyzed to give compounds VI‐IX.
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