Substitution reactions with 2-methoxy- and 2-ethoxy-1-naphthylamines

F. Bell

Research output: Contribution to journalArticle

Abstract

Substitution experiments with the acetyl, formyl, and toluene-p-sulphonyl derivatives of 2-methoxy- and 2-ethoxy-1-naphthylamines show that, whereas chlorination and nitration proceed mainly, or even exclusively, in position 4, yet bromination may yield the 6-derivative as the main product. A comparison is made with the results of substitution experiments with 2:6-xylidine.

Original languageEnglish
Pages (from-to)519-525
Number of pages7
JournalJournal of the Chemical Society (Resumed)
Publication statusPublished - 1959

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