Title of article
A deeper insight into direct trifluoromethoxylation with trifluoromethyl triflate
Author/Authors
Marrec، نويسنده , , Olivier and Billard، نويسنده , , Thierry and Vors، نويسنده , , Jean-Pierre and Pazenok، نويسنده , , Sergii and Langlois، نويسنده , , Bernard R.، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2010
Pages
8
From page
200
To page
207
Abstract
Commercially available fluorides (silver fluoride and n-tetrabutylammonium triphenyldifluorosilicate), combined with TFMT, allow a simple generation, in situ, of silver and n-tetrabutylammonium trifluoromethoxides which were able to react with electrophilic substrates. Silver trifluoromethoxide, which is usually more efficient than n-tetrabutylammonium trifluoromethoxide, converts, under mild conditions, primary aliphatic bromides and iodides, as well as primary and secondary benzylic or allylic bromides to the corresponding trifluoromethoxylated compounds. Several trifluoromethyl ethers, which could be valuable building-blocks, were prepared in such a way.
Keywords
Trifluoromethyl trifluoromethanesulfonate , Trifluoromethoxy-substitued compounds , Trifluoromethoxylation , Trifluoromethoxide , Trifluoromethyl triflate
Journal title
Journal of Fluorine Chemistry
Serial Year
2010
Journal title
Journal of Fluorine Chemistry
Record number
1610792
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