149379-76-0Relevant academic research and scientific papers
Synthesis of substituted benzenes from α-methylene ketones
Khaidem, Ibomacha Singh,Singh, Sagolsem Lokhol,Singh, Laishram Ramananda,Khan, Mohd Ziaur Rahman
, p. 911 - 914 (2007/10/03)
A new general method for the synthesis of substituted benzenes from cyclic ketones having active methylene groups via the corresponding hydroxymethylene ketones and enamino-ketones has been developed. Formylation of these ketones with ethyl formate followed by enamination with pyrrolidine produces enamino-ketones which on reaction with threefold excess of malononitrile in boiling benzene in the presence of ammonium acetate in acetic acid gives the substituted benzenes in good yield. The reaction has been extended to aliphatic and aromatic ketones having active methylene groups to give substituted benzenes and biphenyls, respectively.
A Simple Synthesis of 2-Methoxypyridine-3-carbonitriles
Victory, Pedro,Borrell, Jose I.,Vidal-Ferran, Anton
, p. 769 - 776 (2007/10/02)
The condensation of propanedinitrile with several enals or enones in a methanol-sodium methoxide system provides a one-step route to 2-methoxypyridine-3-carbonitriles.Together with these compounds substituted 2-aminobenzene-1,3-dicarbonitriles, were obtained as by-products.
SYNTHESIS OF 4-AMINO-8-CYANOQUINAZOLINES FROM ENONES AND ENALS
Victory, Pedro,Borrell, Jose I.,Vidal-Ferran, Anton,Montenegro, Elvira,Jimeno, M. Luisa
, p. 2273 - 2280 (2007/10/02)
The treatment in a sodium methoxide/methanol solution of α,β-unsaturated enones or aldehydes with propanedinitrile in a 1:2 molar ratio led to 2-aminobenzene-1,3-dicarbonitriles.These compounds afforded 4-amino-8-cyanoquinazolines by reaction with formamide or guanidine.
