TY - JOUR
T1 - Synthesis of bis-imidazole derivatives from 2,6-bis(4-formylbenzylidiene)-cycloalkanones
AU - Hoseini-Ghazvini, Mohammad Bagher
AU - Mobinikhaledi, Akbar
PY - 2014/11
Y1 - 2014/11
N2 - 2,5-Bis(4-(4,5-bis(4-aryl)-1H-imidazol-2-yl)benzylidene)-cycloalkanones were synthesised by reacting 4,4′-(2-oxocycloalkane-1,3-diylidene) bis(methan-1-yl-1-ylidene) dibenzaldehydes, resulting from aldol condensation of terephthalaldehyde and cycloalkanones, with benzil and ammonium acetate. The structures of the products were then identified by FTIR, 1H NMR, 13C NMR and elemental analysis. The reaction conditions were optimised by varying the type and amount of catalyst, and temperature. The key advantages of this process are simple procedure, environmentally friendly conditions and good yield of products.
AB - 2,5-Bis(4-(4,5-bis(4-aryl)-1H-imidazol-2-yl)benzylidene)-cycloalkanones were synthesised by reacting 4,4′-(2-oxocycloalkane-1,3-diylidene) bis(methan-1-yl-1-ylidene) dibenzaldehydes, resulting from aldol condensation of terephthalaldehyde and cycloalkanones, with benzil and ammonium acetate. The structures of the products were then identified by FTIR, 1H NMR, 13C NMR and elemental analysis. The reaction conditions were optimised by varying the type and amount of catalyst, and temperature. The key advantages of this process are simple procedure, environmentally friendly conditions and good yield of products.
KW - Aldol condensation
KW - Bis-imidazole
KW - Green chemistry
KW - Multicomponent reaction
KW - Solvent-free conditions
UR - http://www.scopus.com/inward/record.url?scp=84918540847&partnerID=8YFLogxK
U2 - 10.3184/174751914X14118009994979
DO - 10.3184/174751914X14118009994979
M3 - Article
AN - SCOPUS:84918540847
SN - 1747-5198
VL - 38
SP - 648
EP - 650
JO - Journal of Chemical Research
JF - Journal of Chemical Research
IS - 11
ER -