2015
DOI: 10.17159/0379-4350/2015/v68a3
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A solvent-free synthesis of polyhydroquinolines via Hantzsch multicomponent condensation catalyzed by nanomagnetic-supported sulfonic acid

Abstract: A simple and efficient procedure for the synthesis of polyhydroquinolines was developed, involving a one-pot four-component Hantzsch condensation of aromatic aldehydes, 1,3-cyclohexanediones, alkyl acetoacetate and ammonium acetate in the presence of a catalytic amount of nanomagnetic-supported sulfonic acid under solvent-free conditions. The method offers several advantages including high yields, short reaction times, a simple work-up procedure and catalyst reusability for several runs. Furthermore, easy isol… Show more

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Cited by 31 publications
(7 citation statements)
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“…Higher temperatures resulted into the decrease in the yield of the desired product because of the formation of byproducts as observed by TLC. [88] Further, in order to investigate the effect of the solvents on the reaction, screening of the different solvents varying from polar to non-polar was done. For this, the reaction was performed at room temperature using 10 mg of catalyst in the presence of 4 ml of different solvents such as EtOH, MeOH, H 2 O, EtOH:H 2 O (1 : 1), MeOH:H 2 O (1 : 1), acetonitrile, DCM, THF and toluene.…”
Section: Catalytic Application Of Lfo Nps In the Synthesis Of Functiomentioning
confidence: 99%
“…Higher temperatures resulted into the decrease in the yield of the desired product because of the formation of byproducts as observed by TLC. [88] Further, in order to investigate the effect of the solvents on the reaction, screening of the different solvents varying from polar to non-polar was done. For this, the reaction was performed at room temperature using 10 mg of catalyst in the presence of 4 ml of different solvents such as EtOH, MeOH, H 2 O, EtOH:H 2 O (1 : 1), MeOH:H 2 O (1 : 1), acetonitrile, DCM, THF and toluene.…”
Section: Catalytic Application Of Lfo Nps In the Synthesis Of Functiomentioning
confidence: 99%
“…[62][63][64] Synthesis of polyhydroquinoline derivatives is an interesting research challenge to synthetic chemists. Several improved methods for the synthesis of polyhydroquinoline derivatives such as CoFe 2 O 4 @Pr, [65] molecular iodine, [66] Fe 3 O 4 @chitosan, [67] Thiamine hydrochloride (Vitamin-B 1 ), [68] Amberlite IRA 900, [69] Nano-g-Fe 2 O 3 -SO 3 H, [70] p-toluenesulfonic acids, [71] Sulfamic acids (NH 2 SO 3 H), [72] SiO 2 @Fe 3 O 4 , [73] Gd(OTf) 3 , [74] and Fe 3 O 4 -SA-PPCA [75] have been reported. However, these procedures suffer some drawbacks still exist, such as volatile organic solvents, long reaction time, low yields, expensive catalysts, critical product isolation, and catalyst recycling.…”
Section: Recycling Study Of the Catalystmentioning
confidence: 99%
“…Michael addition occurs between the imine intermediate and 5,5‐dimethyl‐1,3‐cyclohexanedione and then further cyclisation yields the required 1,4‐dihydropyridine in a short span (>20 min) (Scheme ). Nano‐γ‐Fe 2 O 3 ‐SO 3 H was employed by Otokeshn et al., under solvent free condition at a 60 °C for 65 min, the activity of catalyst is up to 5 cycles and the product yield is 89–98 %.Thus V 2 O 5 /ZrO 2 serves as an sustainable catalyst in the synthesis of substituted 1,4‐dihydropyridine derivatives, which are widely used as a calcium channel blockers, under room temperature conditions.…”
Section: Zirconia Supported Mixed Oxidesmentioning
confidence: 99%