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Synthesis 2004(7): 986-988
DOI: 10.1055/s-2004-822322
DOI: 10.1055/s-2004-822322
SHORTPAPER
© Georg Thieme Verlag Stuttgart · New York
A New and Facile Method for Stereoselective Synthesis of (E)-Styryl Bromides by the Reduction of 1,1-Dibromoalkenes Using LiAlH4-EtOAc (1:1)
Weitere Informationen
Received
2 February 2004
Publikationsdatum:
14. April 2004 (online)
Publikationsverlauf
Publikationsdatum:
14. April 2004 (online)
Abstract
A facile method for stereoselective synthesis of (E)-styryl bromides by the reduction of 1,1-dibromoalkenes using LiAlH4-EtOAc (1:1) is described. We believe that the present procedure is a good alternative to the Tokuda’s microwave method with good stereoselectivity.
Key words
1,1-dibromoalkenes - LiAlH4-EtOAc - styryl bromides
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The use of other reagents, such as Li(i-Bu)2BuAlH, LiEt3BH and Li(s-Bu)3BH, gave less satisfactory results. In the case of NaBH4, no reaction occurred.
15When the reaction time was made longer from 2 h to 7 h, an increase in the ratio of the styrene was observed as shown below (Scheme [1] ).