Informations sur le produit
- benzamide, N-(4-bromophenyl)-
N-Benzyl-4-bromoaniline is a chemical compound which has minimal reactivity with amines and imines. It is also able to react with aldehydes, ketones, alcohols, esters, and carboxylic acids. The product of the reaction is an aldimine or a secondary amine. This type of reaction was first discovered in 1894 by Emil Fischer. N-Benzyl-4-bromoaniline can be used as a catalyst for hydroboration reactions because it does not react with functional groups that are sensitive to hydroboration such as carbonyl compounds and nitro compounds.
The reaction mechanism for this type of reaction is an oxidative addition that forms the intermediate enamine. This enamine reacts with the electrophilic partner to form either an imine or an aldimine. The hydroboration then occurs when the hydrogen on BH3 attacks the iminium ion
Propriétés chimiques
Question d’ordre technique sur : 3D-CAA87983 N-Benzyl-4-bromoaniline
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