Literature DB >> 23682199

Benzamide synthesis by direct electrophilic aromatic substitution with cyanoguanidine.

Rajasekhar Reddy Naredla1, Douglas A Klumpp.   

Abstract

Cyanoguanidine is an inexpensive commodity chemical and it is found to be a useful reagent for the direct Friedel-Crafts carboxamidation of arenes. The reaction works best in an excess of Brønsted superacid, an observation suggesting the involvement of a superelectrophilic intermediate. Theoretical calculations indicate that the most stable diprotonated species involves protonation at the guanidine and cyano nitrogen atoms.

Entities:  

Keywords:  Friedel-Crafts; benzamide; carboxamidation; superacid; superelectrophile

Year:  2012        PMID: 23682199      PMCID: PMC3652529          DOI: 10.1016/j.tetlet.2012.06.135

Source DB:  PubMed          Journal:  Tetrahedron Lett        ISSN: 0040-4039            Impact factor:   2.415


  7 in total

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7.  Superelectrophilic chemistry of amino-nitriles and related substrates.

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  7 in total
  2 in total

1.  A Lewis Acid Catalyzed annulation to 2,1-benzisoxazoles.

Authors:  Kate D Otley; Jonathan A Ellman
Journal:  J Org Chem       Date:  2014-08-26       Impact factor: 4.354

2.  Solid-state Reaction of Azolium Hydrohalogen Salts with Silver Dicyanamide--Unexpected Formation of Cyanoguanidine-azoles, Reaction Mechanism and Their Hypergolic Properties.

Authors:  Wei Liu; Qiu-han Lin; Yu-chuan Li; Peng-wan Chen; Tao Fang; Ru-bo Zhang; Si-ping Pang
Journal:  Sci Rep       Date:  2015-06-03       Impact factor: 4.379

  2 in total

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