Author:
Elder John W.,Mariella Raymond P.
Abstract
3,5-Di-tert-butylphenol (I) was synthesized by two independent routes. It was possible to isolate a mononitro and a dinitro product. It was not possible to isolate a trinitrated product (3,5-di-tert-butylpicric acid). Bromination of I gave the dibrominated product, and chlorination of I gave a dichlorinated product and a tetrachloro product; the latter was shown to possess the dieneone structure.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
17 articles.
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