Journal of Synthetic Organic Chemistry, Japan
Online ISSN : 1883-6526
Print ISSN : 0037-9980
ISSN-L : 0037-9980
Aromatic Substitutions by the Aryl Radicals. IX
p-Methylphenylations of Anisole and Toluene, and Phenylation of Chlorobenzene
Toshihiko MIGITA
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1961 Volume 19 Issue 11 Pages 840-844

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Abstract
The determination, by means of isotope dilution analysis of the molar ratio of p-methyl (14C)-biphenyl, 2-methoxy-4′-methyl ('4C)-biphenyl, 3-methoxy-4, -melhyl (14C)-biphenyl, and 4-methoxy-4′-methyl (14C)-biphenyl formed through the reaction of N-nitroso-p-methyl (14C)-acetanilide in an equimolar mixture of anisole and benzene, is described. From the results, the partial rate factors of the ortho, meta and para positions of anisole for the homolytic p-methylphenylation were found to be 3.69, 1.09 and 1.52, respectively. Partial rate factors for toluene, 3.27, 1.00 and 1.33 were obtained from the results of experiments in a mixture of toluene and benzene.
A similar experiment on the reaction of N-nitrosoacetanilide-(phenyl-14C) in a mixture of chlorobenzene and benzene gave partial rate factors of the ortho, meta and para positions of chlorobenzene for the phenylation, 3.09, 1.01 and 1.48, respectively.
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© The Society of Syhthetic Organic Chemistry, Japan
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