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Iodine(III)-mediated umpolung of bromide salts for the ethoxybromination of enamides.

Organic letters (2013-04-02)
Sophie Nocquet-Thibault, Pascal Retailleau, Kevin Cariou, Robert H Dodd
ZUSAMMENFASSUNG

Using (diacetoxyiodo)benzene in conjunction with simple bromide salts in ethanol allows the regioselective ethoxybromination of a wide range of enamides, thus yielding highly versatile α-bromo hemiaminals, which can then be engaged in a broad array of transformations.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Lithiumbromid, ReagentPlus®, ≥99%
Sigma-Aldrich
Lithiumbromid -Lösung, 54 wt. % in H2O
Sigma-Aldrich
Lithiumbromid, powder and chunks, ≥99.995% trace metals basis
Sigma-Aldrich
Lithiumbromid, AnhydroBeads, −10 mesh, 99.999% trace metals basis
Sigma-Aldrich
Lithiumbromid, AnhydroBeads, −10 mesh, ≥99.9% trace metals basis