Author:
Rosenthal Alex,Weir Mary R. S.
Abstract
The reaction of benzophenone phenylhydrazone with carbon monoxide at 230° and 3800 p.s.i. to give 3-phenylphthalimidine-N-carboxyanilide, and at lower temperatures (190–220°) to give a mixture of 3-phenylphthalimidme-N-carboxyanilide and 3-phenylphthalimidine has been studied. An independent synthesis of 3-phenylphthalimidine-N-carboxyanilide is described. 4-Methylbenzophenone phenylhydrazone reacted with carbon monoxide to give a mixture of two isomers, 3-phenyl-6-methylphthalimidine-N-carboxyanilide and 3-(p-tolyl)-phthalimidine-N-carboxyanilide, whose infrared spectra are described. An independent synthesis of 3-(p-tolyl)phthalimidine-N-carboxyanilide has also been carried out.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
12 articles.
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