2012
DOI: 10.1016/j.apcata.2012.04.011
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A highly efficient and reusable heterogeneous catalyst for the one-pot synthesis of tetrasubstituted imidazoles

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Cited by 34 publications
(16 citation statements)
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“…[21][22][23][24] Various protocols for preparation of imidazoles via multicomponent reaction have been tested in literature, which employs a three-component reaction of 1,2-diketone or ketomonoxime, aldehyde, and ammonium acetate, or four-component reaction of 1,2-diketone, aldehyde, primary amines, and ammonium acetate. [25][26][27][28] Many of the synthetic approaches for the preparation of imidazoles suffer from one or more drawbacks such as drastic reaction conditions, low yields, by-products, prolonged reaction time, volatile organic solvent, tedious work-up processes, expensive and unrecyclable catalysts. [29][30][31][32] Thus, the development of efficient and environmentally benign catalysts is still highly desirable.…”
Section: Introductionmentioning
confidence: 99%
“…[21][22][23][24] Various protocols for preparation of imidazoles via multicomponent reaction have been tested in literature, which employs a three-component reaction of 1,2-diketone or ketomonoxime, aldehyde, and ammonium acetate, or four-component reaction of 1,2-diketone, aldehyde, primary amines, and ammonium acetate. [25][26][27][28] Many of the synthetic approaches for the preparation of imidazoles suffer from one or more drawbacks such as drastic reaction conditions, low yields, by-products, prolonged reaction time, volatile organic solvent, tedious work-up processes, expensive and unrecyclable catalysts. [29][30][31][32] Thus, the development of efficient and environmentally benign catalysts is still highly desirable.…”
Section: Introductionmentioning
confidence: 99%
“…Nitrogen of ammonia attacked as a nucleophile at the protonated carbonyl group of aldehydes, and the diamine intermediate was formed. Benzil and diamine intermediate condensed to cyclic intermediate state which rearranged by a [1,5]‐H shift to the trisubstituted imidazoles …”
Section: Resultsmentioning
confidence: 99%
“…Benzil and diamine intermediate condensed to cyclic intermediate state which rearranged by a [1,5]-H shift to the trisubstituted imidazoles. [40][41][42]…”
Section: Resultsmentioning
confidence: 99%
“…Recently, four-component condensation of benzil, benzaldehyde derivatives, primary amines, and ammonium acetate has been reported for this system using silicagel or zeolite HY [16], silicagel, NaHSO 4 [17], molecular iodine [18], K 5 CoW 12 O 40 ,3H 2 O [19], Keggin, Preyssler, and Wells-Dawson-type heteropolyacids [20][21][22], MCM-41 [23], HClO 4 -SiO 2 [24], BF 3 , SiO 2 [25], poly(AMPS-co-AA) [26], L-proline [27] high surface area [28], and InCl 3 , 3H 2 O [29], DABCO [30], Al 2 O 3 [31], MPS [32], zeolite Cu(NO 3 ) 2 [33], SBPPSA [34], N-methyl-2-pyrrolidonium hydrogen sulfate [35], PEG-400 [36], NaH 2 PO 4 [37], TFA [38], carbon based/solid acid [39], [Bmim]Br [40], Fe +3 -K10 [41], CU(OAc) 2 [42], CAN [43], FeCl 3 [44], NiCl 2 ⋅ 6H 2 O [45], Bronsted acidic ionic liquids [46], ZrCl 4 [47], and solid acid zirconium nanocatalyst [48]. ese methods have their own merits and drawbacks.…”
Section: Introductionmentioning
confidence: 99%