N-aryl-N-phenylhydroxylamines from phenylmagnesium bromide and nitro-compounds

Yul Yost; H. R. Gutmann; C. C. Muscoplat

doi:10.1039/J39710002119

N-aryl-N-phenylhydroxylamines from phenylmagnesium bromide and nitro-compounds

Yul Yost, H. R. Gutmann, C. C. Muscoplat

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30 Scopus citations

Abstract

N-Aryl-N-phenylhydroxylamines were prepared from phenylmagnesium bromide and aryl nitro-compounds. The hydroxylamines were then reduced to secondary amines. The isolation of phenol as a by-product in the former reaction supports the suggested mechanism.

Original language	English (US)
Pages (from-to)	2119-2122
Number of pages	4
Journal	Journal of the Chemical Society C: Organic Chemistry
DOIs	https://doi.org/10.1039/J39710002119
State	Published - 1971

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title = "N-aryl-N-phenylhydroxylamines from phenylmagnesium bromide and nitro-compounds",

abstract = "N-Aryl-N-phenylhydroxylamines were prepared from phenylmagnesium bromide and aryl nitro-compounds. The hydroxylamines were then reduced to secondary amines. The isolation of phenol as a by-product in the former reaction supports the suggested mechanism.",

author = "Yul Yost and Gutmann, {H. R.} and Muscoplat, {C. C.}",

year = "1971",

doi = "10.1039/J39710002119",

language = "English (US)",

pages = "2119--2122",

journal = "Journal of the Chemical Society C: Organic Chemistry",

issn = "0022-4952",

publisher = "Chemical Society",

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TY - JOUR

T1 - N-aryl-N-phenylhydroxylamines from phenylmagnesium bromide and nitro-compounds

AU - Yost, Yul

AU - Gutmann, H. R.

AU - Muscoplat, C. C.

PY - 1971

Y1 - 1971

N2 - N-Aryl-N-phenylhydroxylamines were prepared from phenylmagnesium bromide and aryl nitro-compounds. The hydroxylamines were then reduced to secondary amines. The isolation of phenol as a by-product in the former reaction supports the suggested mechanism.

AB - N-Aryl-N-phenylhydroxylamines were prepared from phenylmagnesium bromide and aryl nitro-compounds. The hydroxylamines were then reduced to secondary amines. The isolation of phenol as a by-product in the former reaction supports the suggested mechanism.

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UR - http://www.scopus.com/inward/citedby.url?scp=37049115539&partnerID=8YFLogxK

U2 - 10.1039/J39710002119

DO - 10.1039/J39710002119

M3 - Article

AN - SCOPUS:37049115539

SN - 0022-4952

SP - 2119

EP - 2122

JO - Journal of the Chemical Society C: Organic Chemistry

JF - Journal of the Chemical Society C: Organic Chemistry

ER -

N-aryl-N-phenylhydroxylamines from phenylmagnesium bromide and nitro-compounds

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