Nouvelles Méthodes de Déshalogènation et de Formation D'Éthers D'Enol Triméthylsilyliques Par Action de iPr2NLi Sur Quelques α-Monobromo-Et α, α'-Dibromocétones

Autor: Claude Lion, Khadija Lebbar, Jacques-Emile Dubois
Rok vydání: 2010
Předmět:
Zdroj: Bulletin des Sociétés Chimiques Belges. 95:119-126
ISSN: 0037-9646
Popis: Attemps to prepare 2-bromo-2, 4-dimethyl, 3-trimethylsiloxy 3-pentene reacting lithium diisopropylamide (LDA) with 2-bromo-2, 4-dimethyl-3 pentanone have revealed two new reactions. After a few minutes quantitative yields are obtained of either the dehalogenated ketone (after hydrolysis) or the trimethylsilyl enol ether (after addition of trimethylsilyl chloride). These reactions are general and have been extended to other α-monobromoketones and α,α'-dibromoketones. In the latter case, the reaction is more complex and leads generally to dehalogenation or reduction products.
Databáze: OpenAIRE