## 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 apprec
✦ LIBER ✦
Action du sodium sur les phénylimino-éthers. I. Condensation des éthers phénylimino-benzoïques
✍ Scribed by Roland Jaunin; Gabriel Séchaud
- Publisher
- John Wiley and Sons
- Year
- 1954
- Tongue
- German
- Weight
- 410 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
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 postulated.
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## Abstract Ethenic alcohols, ethynic tertiary alcohols, hydroxy ethers, cyclic alcohols, araliphatic alcohols, and phenol react very easily with phenyl phosphonic oxide to yield the corresponding phosphonic monoesters.