Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Schmidt reactions synthetic utility

Crossed aldol condensations, where both aldehydes (or other suitable carbonyl compounds) have a-H atoms, are not normally of any preparative value as a mixture of four different products can result. Crossed aldol reactions can be of synthetic utility, where one aldehyde has no a-H, however, and can thus act only as a carbanion acceptor. An example is the Claisen-Schmidt condensation of aromatic aldehydes (98) with simple aliphatic aldehydes or (usually methyl) ketones in the presence of 10% aqueous KOH (dehydration always takes place subsequent to the initial carbanion addition under these conditions) ... [Pg.226]


See other pages where Schmidt reactions synthetic utility is mentioned: [Pg.223]    [Pg.284]    [Pg.223]    [Pg.449]    [Pg.109]    [Pg.268]    [Pg.359]    [Pg.109]    [Pg.145]    [Pg.308]    [Pg.202]    [Pg.109]    [Pg.123]   
See also in sourсe #XX -- [ Pg.363 , Pg.364 , Pg.365 , Pg.366 , Pg.367 , Pg.368 , Pg.379 , Pg.391 ]




SEARCH



Schmidt

Schmidt reaction

Schmidt reaction reactions

Synthetic reactions

Synthetic utility

© 2024 chempedia.info