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Methoxycarbonylation of Iodobenzene in Ionic Liquids. A Case of Inhibiting Effect of Imidazolium Halides
Author(s) -
Zawartka W.,
Trzeciak A. M.,
Ziółkowski J. J.,
Lis T.,
Ciunik Z.,
Pernak J.
Publication year - 2006
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.200606142
Subject(s) - chemistry , ionic liquid , iodobenzene , medicinal chemistry , palladium , catalysis , pyridinium , yield (engineering) , bromide , carbonylation , imidazole , halide , inorganic chemistry , organic chemistry , carbon monoxide , materials science , metallurgy
The palladium( II ) complexes, PdCl 2 (cod) ( 1 ), PdCl 2 [P(OPh) 3 ] 2 ( 2 ), [bmim] 2 [PdCl 4 ] ( 3 ), and [bmpy] 2 [PdCl 4 ] ( 4 ) (bmim=1‐butyl‐3‐methylimidazolium cation, bmpy=1‐butyl‐4‐methylpyridinium cation), were found to be active catalysts for the methoxycarbonylation of iodobenzene in ionic liquid (IL) media. The best results were obtained in pyridinium salts, [bmpy]X (X=Cl, Br, BF 4 , PF 6 ) (76–100 % yield). In methoxycarbonylation reactions carried out in imidazolium salts, [bmim]BF 4 and [bmim]PF 6 , the yield of benzoic acid methyl ester was slightly lower (50–78 % yield), whereas in [bmim]X (X=Cl, Br) the reaction was totally retarded. The inhibiting effect was not observed when a Me group was present at C‐2 (instead of a proton) on the imidazole ring. A palladium‐carbene complex, Pd(bmimy) 2 Br 2 ( 5 ), obtained in the reaction of a palladium catalyst precursor with [bmim]Cl, presented much lower activity than precursors 1–4 . Its formation may explain the observed inhibition of methoxycarbonylation in a [bmim]Cl medium.