NaHSO<sub>4</sub>/SiO<sub>2</sub>: An Efficient Catalyst for the Synthesis of β-Enaminones and 2-Methylquinolin-4(1H)-Ones under Solvent-Free Condition
NaHSO4/SiO2: An Efficient Catalyst for the Synthesis of β-Enaminones and 2-Methylquinolin-4(1H)-Ones under Solvent-Free Condition
Journal of the Korean Chemical Society. 2010. Dec, 54(6): 723-726
Copyright © 2010, The Korean Chemical Society
  • Received : April 05, 2010
  • Accepted : August 23, 2010
  • Published : December 20, 2010
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Suryakant B., Sapkal
Kiran F., Shelke
Bapurao B., Shingate
Murlidhar S., Shingare

An efficient and simplified protocol for NaHSO 4 /SiO 2 catalyzed solvent-free synthesis of β-enaminone and 2-methylquinolin-4(1H)-one derivatives under microwave irradiation is described. A series of functionalized derivatives have been synthesized in shorter reaction times with moderate to good yields. The use of milder catalyst in non-conventional method offers significant advantages over conventional methods, such as higher selectivities, simplicity, solvent-free reaction and non-environmental polluting conditions.
Nitrogen containing organic compounds are of special interest because they constitute an important class of natural and non-natural products, many of which exhibit useful biological activities. Among those compounds, β-enaminones have been employed as synthetic building block of a wide veriety of heterocycles, 1 key intermediate in synthesis of different heterocycles and naturally occouring alkaloids 2 and in pharmaceuticles. 3 Despite the importance of β-enaminones as valuable biologically active compounds, their synthesis has received great attention of chemists and hence several routes have been recently reported in literature using Lewis acids, 4 P 2 O 5 /SiO 2 , 5 Cu-nanoparticles, 6 and heteropoly acid. 7 In addition, β-enaminone have also been synthesized by using non-traditional methods. 8
Another nitrogen containing heterocyclic compound is quinoline moiety. Quinolines possess diverse biological as well as physiological activities such as, anti-malerial, antituberculosis, antagonists and anti-cancer activity. 9 Realizing the importance of quinoline molecule, several methods have been reported in literature such as, by the condensation of o-amino aldehyde/ketones, 10 Skraup, 11 Knorr, 12 Conard-Limpach, 13 Dober-Vonmiller, 14 Combs, 15 Friedlander 16 etc. Moreover, H 2 SO 4 , 17 AcOH/CaSO 4 in Ph 2 O at 250 ℃ 17 and P -TsOH in EtOH/xylene at 250 ℃ 19 has been recently reported.
Unfortunately many of these methods for the synthesis of β-enaminones and quinolines suffers from relevant limitations such as, drastic condition, low product yield, tedious work-up procedure, low selectivity, and required chromatographic isolation technique. Therefore, search of new simple, clean and one-pot method for the synthesis of desired organic compounds is of prime interest. In search of better alternatives, we have paid attention to find convenient and efficient method based on green approach for the synthesis of β-enaminones and quinoline-4-one derivatives.
Solvent-free reactions have attracted much attention in organic synthesis in recent years, 20 not only because solventfree reactions offers practical advantages over reactions in organic solvents from economical, environmental and safety standpoints, but also because solvent-free reactions usually need shorter reaction time, low costs, simplicity in process, handling and no need to use harmful organic solvents. These factors are beneficial to industry as well as to environment. Thus solvent-free reactions are one of the most important synthesis techniques in green chemistry. Various solvent-free reactions were found to occurs using microwave irradiation. 21 Microwave irradiation takes a particular place being an emerging technique that provides an alternative to conventional heating by introducing energy into chemical reaction. Hence microwave technique has been successfully applied because of some advantages such as, very fast heating, better homogeneity in reaction temperature, shorter reaction time, improved conversion and clean product formation. Therefore, we would like to report the solvent-free synthesis of β-enaminones and 4-quinolones under microwave irradiation.
All starting materials and reagents were commercially available and used without further purification. All the melting points were taken in an open capillary and are uncorrected. The progress of the reactions was monitored by thin layer chromatography (TLC). IR spectra were recorded on Perkin-Elmer FT-IR spectrophotometer in KBr disc. 1 H NMR spectra were recorded on mercury plus Varian spectrometer at 400 MHz in DMSO- d 6 as a solvent and chemical shift values are recorded in units δ (ppm) relative to tetramethylsilane (Me 4 Si) as an internal standard.
- Synthesis of β-enaminones
A mixture of aromatic amines (1 mmol), dimedone (1 mmol) and NaHSO 4 /SiO 2 (0.5 g) were taken in a beaker. The reaction mixture homogenized with the help of glass rod and irradiated in microwave oven (180 W) by the interval of 10 second. The progress of reaction was monitored on TLC. After completion of the reaction, mixture was cooled to room temperature and poured on crushed ice. Thus, solid obtained was filtered, dried and purified by crystallization in ethanol.
- Synthesis of 2-methylquinolin-4(1H)-ones
A mixture of anilines (1 mmol), ethyl acetoacetate (1 mmol) and NaHSO 4 /SiO 2 (0.5 g) were taken in beaker. The reaction mixture was homogenized with the help of glass rod and irradiated under microwave oven (360 W) by interval of 10 second. After completion of the reaction as indicated on TLC. The reaction mixture was cooled at room temperature and poured on crushed ice. Thus, solid obtained was filtered, dried and purified by crystallization in ethanol.
In continuation of our research work on microwave assisted organic reactions for the synthesis of various bioactive compounds, 20a , 22 herein an effective strategies catalyzed by NaHSO 4 /SiO 2 under microwave irradiation have been discussed.
Initially we examined the efficiency of different catalysts for the condensation reactions of aniline with dimedone as representative reactants under microwave irradiation at 180 W ( 1 ).
Our initial investigation focused on the use of acidic catalyst such as Lewis acids, acidic salts for the synthesis of β-enaminones by the condensation of the reactants. In search of an efficient catalyst and the best experimental condition, the preferred reactions in the presence of catalyst at 180 W have been considered. After successful screening of different catalysts shown in 1 , it has been found that acidic salt NaHSO 4 in combination with SiO 2 as a solid support act as a best promoter for this reaction and gives 90% product yield within 4 min ( 1 , entry 7). This amazing result is may be due to NaHSO 4 act as Brønsted acid which protonate carbonyl oxygen of dimedone to enhance the electrophilicity of that carbonyl carbon preferably on the active solid support of SiO 2 to afford respective product yield. Such type of stepping-up performance about other catalysts was not observed ( 1 , entries 1-4).
Screening of different catalyst for the synthesis of β-enaminones
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aIsolated yield
Synthesis of β-enaminone derivatives catalyzed by NaHSO4/SiO2
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aIsolated product yield and all products were characterized from their spectroscopic (IR,1H NMR and MS) data and compared with authentic samples.
Screening of suitable catalyst for the synthesis of 4-quinolones
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aIsolated yield
Meanwhile, MgSO 4 , Na2SO 4 , TiO 2 , and ZnCl 2 have also been screened and required longer reaction time under microwave irradiation and conversion of reactant into corresponding products is less (> 20 - 40%). Even though use of NaHSO 4 or SiO 2 does not results into higher yield as it has given in combination of NaHSO 4 /SiO 2 ( 1 , entry 5, 6). Herein we would like to report the combination of catalysts NaHSO 4 /SiO 2 as a best catalyst for the synthesis of β-enaminone derivatives under microwave irradiation.
Our next attempt was to perform synthesis of 4-quinolone derivatives by the cyclocondensation of aromatic anilines with ethyl acetoacetate under solvent-free condition. The catalytic influence of various inorganic solid supports on the condensation of aniline with ethyl acetoacetate under microwave irradiation at 360 W has studied and the results are as shown in 3 .
Synthesis of 4-quinolone derivatives catalyzed by NaHSO4/SiO2
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aIsolated product yield and all products were characterized from their spectroscopic (IR,1H NMR and MS) data and compared with authentic samples.
In order to select an appropriate catalyst for the synthesis of 4-quinolones under solvent-free condition, initially we have screened the acidic clays such as, EPZ-10 and EPZG for the preferred reaction, it was observed that no significant product was formed even after 30 min ( 3 , entries 1,2). Moreover, starting materials were subjected with MgSO 4 , Na 2 SO 4 as compared to acidic clays; these gives more yield ( 3 , entries 3,4). In addition, we examined the TiO 2 , Al 2 O 3 , and SiO 2 among these SiO 2 gives appreciable yield within 15 min ( 3 , entry 7). Fortunately, we think over acidic salt like NaHSO 4 and applied for the same reaction under microwave irradiation after 10 min 65% reactants were converted into corresponding product. Finally, we decided to use combination of catalyst NaHSO 4 /SiO 2 amazingly, we obtained 92% product yield ( 3 , entry 9). As discussed in earlier results NaHSO 4 /SiO 2 plays same mechanistic role to promote the rate of reaction furnishing better yield within shorter reaction time. When aromatic anilines and ethyl acetoacetate react with each other in the presence of NaHSO 4 /SiO 2 under microwave irradiation, the cyclization of quinoline ring takes place through emine- enamine tautomerization eliminating water molecules we got appreciable yields of desired products within shorter reaction time as shown in 4 .
- Spectral Data for representative compounds
4-Br-enaminone: IR (KBr, cm -1 ): 3264, 1592, 704; 1 H NMR (400, MHz, DMSO- d 6 , δ ppm) 1.02 (6H, s), 2.14 (2H, s), 2.36 (2H, s), 5.13 (1H, s), 6.66 (1H, s broad peak), 6.96 (2H, d, J = 8.6 Hz), 7.39 (2H, d, J = 8.6 Hz); 13 C NMR (DMSO- d 6 , TMS) δ = 26.8,28.5, 31.8, 44.1, 50.4, 100.2, 121.6, 129.8, 132.7, 140.3, 143.2, 198.7; ES-MS: m/z (m+): 393.
2,6-dimethyl-1H-quinolin-4-one: IR (KBr, cm -1 ): 3255; 1628; 1 H NMR (400, MHz, DMSO- d 6 , δ ppm): 2.05 (3H, s); 2.27 (3H, s); 5.99 (1H, s); 7.09 (1H, d, J = 7.5 Hz); 7.38 (1H, t,); 9.10 (1H, s); 13 C NMR (DMSO- d 6 , TMS) δ = 20.87, 29.70, 98.51, 114.73, 120.26, 122.58, 126.43, 129.45, 134.20, 163.72, 205.03; ES-MS: m/z (m+): 173.
In conclusion, we have described simple, efficient and one-pot synthesis of some β-enaminones and quinoline-4-one derivatives under microwave irradiation in the presence of NaHSO 4 /SiO 2 as a catalyst. The synthetic utility of the methodologies demonstrated in this work, whilst contributing the part of green and clean chemistry to sustain the human health and environment unaffected. The remarkable advantages offered by the methods presented are use of safer and ecofriendly catalysts, mild reaction conditions, simplicity of the reaction procedure and high yielding strategies.
The authors are thankful to the Head, Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad-431 004, MS, India for providing the laboratory facility, We gratefully acknowledge the financial assistance received for this work from University Grants Commission, New Delhi.
Alan C. , Spivey A. C. , Sirikaran R. , Diaper C. M. , David J. , Turner D. 2003 Org. Biomol. Chem. 1638 -
White J. D. , Lhle D. C. 2006 Org. Lett. 8 1081 -    DOI : 10.1021/ol052955y
Abass M. , Mostafa B. B. 2005 Bioorg. Med. Chem. 13 6133 -    DOI : 10.1016/j.bmc.2005.06.038
Dalpozzo R. R. , Nino A. D. , Nardi M. , Procopio B. A. 2006 Synthesis 7 1127 -    DOI : 10.1055/s-2006-926378
Mohammadizadeh M. R. , Hasaninejad A. , Bahramzadeh M. , Khanjarlou Z. S. 2009 Synth. Commun. 39 1152 -    DOI : 10.1080/00397910802513052
Kidwai M. , Bhardwaj S. , Mishra N. , Bansal V. , Kumar A. , Mozumdar S. 2009 Catal. Commun. 10 1514 -    DOI : 10.1016/j.catcom.2009.04.006
Rafiee E. , Joshaghani M. , Eavani S. , Roshidzadeh S. 2008 Green Chem. 10 982 -    DOI : 10.1039/b803249a
Lee A. S. Y. , Cheng R. Y. 1997 Tetrahedron Lett. 38 443 -    DOI : 10.1016/S0040-4039(96)02321-0
Ridley R. G. 2002 Nature 415 686 -    DOI : 10.1038/415686a
Kiss A. , Potor A. , Hell Z. 2008 Catal. Lett. 125 250 -    DOI : 10.1007/s10562-008-9573-7
Skraup Z. H. 1880 Chem. Ber. 13 2086 -
Hauser C. R. , Reynolds G. A. 1948 J. Am. Chem. Soc. 70 2402 -    DOI : 10.1021/ja01187a025
Conard M. , Limpach L. 1887 Chem. Ber. 20 944 -    DOI : 10.1002/cber.188702001215
Dobner O. , Miller W. 1883 Chem. Ber. 16 246 -
Combes A. 1888 Bull. Soc. Chem. 49 89 -
Friedlander P. 1882 Chem. Ber. 15 2572 -    DOI : 10.1002/cber.188201502219
Farah A. A. , Pietro W. 2001 J. Acta Cryst. E-57 677 -
Morris A. L. C. , Jackson Y. A. 2010 Heterocycles 81    DOI : 10.3987/COM-09-11868
Pain C. , Celanire S. , Guillaumet G. , Joseph B. 2003 Tetrahedron 59 9627 -    DOI : 10.1016/j.tet.2003.09.094
Madje B. R. , Shindalkar S. S. , Ware M. N. , Shingare M. S. 2005 Arkivoc xiv 82 -    DOI : 10.3998/ark.5550190.0006.e10
Arvapalli V. S. , Chen G. , Kosarev S. , Tan E. M. , Xie D. , Yet L. 2010 Tetrahedron Lett. 51 284 -    DOI : 10.1016/j.tetlet.2009.10.137
Sapkal S. B. , Shelke K. F. , Shingate B. B. , Shingar M. S. 2009 Tetrahedron Lett. 50 1754 -    DOI : 10.1016/j.tetlet.2009.01.140