Samarium-promoted one-pot reductive acylation of nitrobenzene to acetanilide

Acetanilide was synthesized from nitrobenzene in the presence of acetic anhydride, acetic acid and samarium by a one-pot procedure in good yield.

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Published inJournal of Shanghai University Vol. 10; no. 3; pp. 277 - 278
Main Author 贾学顺 李清 王晓洪 王海龙 刘晓涛
Format Journal Article
LanguageEnglish
Published 01.06.2006
Subjects
乙酰苯胺
硝基苯
还原酰化
Online AccessGet full text
ISSN1007-6417
1863-236X
DOI10.1007/s11741-006-0129-z

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Abstract Acetanilide was synthesized from nitrobenzene in the presence of acetic anhydride, acetic acid and samarium by a one-pot procedure in good yield.
AbstractList Acetanilide was synthesized from nitrobenzene in the presence of acetic anhydride, acetic acid and samarium by a one-pot procedure in good yield.
Author 贾学顺 李清 王晓洪 王海龙 刘晓涛
AuthorAffiliation Department of Chemistry, College of Sciences, Shanghai University, Shanghai 200444, P.R. China
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samarium, reductive acylation, nitrobenzene, acetanilide.
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Snippet Acetanilide was synthesized from nitrobenzene in the presence of acetic anhydride, acetic acid and samarium by a one-pot procedure in good yield.
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SubjectTerms 乙酰苯胺
硝基苯
还原酰化
Title Samarium-promoted one-pot reductive acylation of nitrobenzene to acetanilide
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