Literature DB >> 16095332

Unexpected, drastic effect of triflic acid on oxidative diacetoxylation of iodoarenes by sodium perborate. A facile and efficient one-pot synthesis of (diacetoxyiodo)arenes.

Md Delwar Hossain1, Tsugio Kitamura.   

Abstract

An easy, safe, and effective method for preparing (diacetoxyiodo)arenes from iodoarenes is presented. Addition of trifluoromethanesulfonic acid (triflic acid) as a promoter causes a drastic increase in the yield of (diacetoxyiodo)arenes in the reaction of iodoarenes with sodium perborate. The reaction of the iodoarenes with sodium perborate in acetic acid in the presence of triflic acid at 40-45 degrees C efficiently generates the corresponding (diacetoxyiodo)arenes in high yields within short time.

Entities:  

Year:  2005        PMID: 16095332     DOI: 10.1021/jo050927n

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Aryliodine (III) Diacetates as Substrates for Pd-Ag Catalyzed Arylation of Alkenes.

Authors:  Nikolai M Evdokimov; Alexander Kornienko; Igor V Magedov
Journal:  Tetrahedron Lett       Date:  2011-08-17       Impact factor: 2.415

Review 2.  Chemistry of polyvalent iodine.

Authors:  Viktor V Zhdankin; Peter J Stang
Journal:  Chem Rev       Date:  2008-12       Impact factor: 60.622

  2 in total

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