Canadian Journal of Chemistry

THE SYNTHESIS AND SUBSTITUTION REACTIONS OF 3, 5-DI-tert-BUTYLPHENOL

JW Elder, RP Mariella

Index: Elder,J.W.; Mariella,R.P. Canadian Journal of Chemistry, 1963 , vol. 41, # 7 p. 1653 - 1656

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Citation Number: 5

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.

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