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Benzaldehyde phenylhydrazones, addition

Benzaldehyde phenylhydrazone with DM AD gave 8% of dimethyl 1,3-diphenylpyrazole-4,5-dicarboxylate (136) together with 35% of trimethyl pyrazoletricarboxylate (138), which the authors suggest is obtained from the primary adduct 137 by Michael addition of a second mole of DMAD followed by cleavage, as shown.129... [Pg.303]

Benzaldehyde shows most of the reactions which are characteristic of aliphatic aldehydes. It reduces an ammonaical solution of silver nitrate, forms addition-products with acid sodium sulphite and with hydrocyanic acid, is converted by nascent hydrogen into an alcohol, and yields an oxime and a phenylhydrazone. [Pg.503]


See other pages where Benzaldehyde phenylhydrazones, addition is mentioned: [Pg.212]    [Pg.93]    [Pg.653]    [Pg.242]    [Pg.5]    [Pg.5]    [Pg.219]   


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