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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title = "Substitution reactions with 2-methoxy- and 2-ethoxy-1-naphthylamines",
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.",
author = "F. Bell",
year = "1959",
language = "English",
pages = "519--525",
journal = "Journal of the Chemical Society (Resumed)",
issn = "0368-1769",
publisher = "Chemical Society",

}

Substitution reactions with 2-methoxy- and 2-ethoxy-1-naphthylamines. / Bell, F.

In: Journal of the Chemical Society (Resumed), 1959, p. 519-525.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Substitution reactions with 2-methoxy- and 2-ethoxy-1-naphthylamines

AU - Bell, F.

PY - 1959

Y1 - 1959

N2 - 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.

AB - 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.

M3 - Article

SP - 519

EP - 525

JO - Journal of the Chemical Society (Resumed)

JF - Journal of the Chemical Society (Resumed)

SN - 0368-1769

ER -