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Nano copper oxide catalyzed synthesis of symmetrical diaryl sulfides under ligand free conditions

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Organic Chemistry Divison-I, Indian Institute of Chemical Technology, Hyderabad-500 607, India
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Associate Editor: I. Marek
Beilstein J. Org. Chem. 2011, 7, 886–891. https://doi.org/10.3762/bjoc.7.101
Received 18 Apr 2011, Accepted 04 Jun 2011, Published 30 Jun 2011
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Abstract

Potassium thiocyanate acts as an efficient sulfur surrogate in C–S cross-coupling reactions mediated by recyclable copper oxide nanoparticles under ligand free conditions. This protocol avoids foul smelling thiols, for the synthesis of a variety of symmetrical diaryl sulfides, via the cross-coupling of different aryl halides with potassium thiocyanate, affording corresponding products in moderate to excellent yields.

Keywords: aryl halides; aryl sulfides; copper oxide; cross-coupling; ligand free; potassium thiocyanate; recyclable

Introduction

After the discovery of copper-promoted Ullmann reaction [1-3] for the construction of carbon-hetero atom bonds, several protocols have been reported over the years to establish C–N, C–O, and C–S linkages. Carbon–sulfur bonds are widespread, occurring in numerous pharmaceutically and biologically active compounds [4-8]. A large variety of aryl sulfides are in use for diverse clinical applications in the treatment of cancer [9], HIV [10,11], Alzheimer’s and Parkinson’s diseases [12].

During the last decades, transition and boron group metals, such as palladium [13-18], nickel [19,20], copper [21-37], iron [38], indium [39,40], lanthanum [41] and cobalt [42] have been used in cross-coupling reactions, developed for the formation of carbon–sulfur bonds. Most of these coupling protocols involve the reaction between thiols and aryl halides, resulting in the formation of C–S bonds. Most of these metal-catalyzed reactions involve volatile and foul-smelling thiols as the main drawback, which leads to environmental and safety problems. To overcome these problems, Zhou [43] and coworkers recently reported an efficient C–S bond formation by the reaction of potassium thiocyanate and aryl halides in the presence of a copper catalyst and a ligand in aqueous medium at 130 °C for 48 h. Tao et al. described the synthesis of diaryl sulfides catalyzed by CuI via cross-coupling between aryl halides and thioacetamide using Cs2CO3 as the base and DMSO–H2O as the solvent at 120 °C [44].

These recently developed protocols involve expensive catalytic systems and ligands [43], long reaction times [43,44], metal contamination of the final product, and non recyclability of the catalyst. This leads to increased costs as well as limiting the scope of the reaction. From the synthetic point of view, it is desirable to find novel recyclable catalytic systems, especially under ligand-free conditions, for the synthesis of such highly useful organic compounds.

In the past few years, considerable efforts have been made in the area of heterogeneous catalysis for various organic transformations. In general, heterogeneous catalysts offer higher surface area and lower coordinating sites, which are responsible for their higher catalytic activity [45-47]. Furthermore, heterogeneous catalysis has the advantage of high atom efficiency, easy product purification, and reusability of the catalyst. However, up until now, the investigation of nanoparticles as catalysts has been limited and will be widely studied in future.

Results and Discussion

In continuation of our investigations on metal-catalyzed cross-coupling reactions, we have explored the CuO-catalyzed synthesis of diaryl sulfides under ligand-free conditions (Scheme 1). To the best of our knowledge, this is the first recyclable copper oxide nanoparticle-catalyzed cross-coupling of aryl halides with potassium thiocyanate [46-51].

[1860-5397-7-101-i1]

Scheme 1: Synthesis of symmetrical aryl sulfides catalyzed by copper oxide nanoparticles.

Initially, the reaction between potassium thiocyanate and iodobenzene was selected as the model reaction for optimizing the reaction conditions involving various copper sources, bases, solvents, and temperature (Table 1).

Table 1: Screening of copper sources for the cross-coupling reaction between iodo benzene and potassium thiocyanate.a

Entry Catalyst Solvent Base T (°) Yield (%)b
1 CuO DMSO K2CO3 rt 0
2 CuO DMSO K2CO3 80 46
3 CuO DMSO K2CO3 130 51
4 CuO DMSO Cs2CO3 130 79
5 CuO DMSO KOH 130 94
6 CuO DMSO K3PO4 130 42
7 CuO Toluene KOH 130 trace
8 CuO H2O KOH 130 trace
9 CuO PEG KOH 130 60
10 CuO DMF KOH 130 70
11 – DMSO KOH 130 0c
12 CuO DMSO – 130 0d
13 CuCl2·2H2O DMSO KOH 130 83
14 CuSO4·5H2O DMSO KOH 130 71
15 Cu(OAc)·H2O DMSO KOH 130 79

aReaction conditions: Iodobenzene (2.0 mmol), potassium thiocyanate (1.5 mmol), nano CuO (5.0 mol %), solvent (2.0 mL), base (2.0 equiv), 130 °C, 20 h. bIsolated yield. cIn the absence of catalyst. dIn the absence of base.

First, several copper catalysts were screened (Table 1), and CuO was found to be promising for this tandem reaction (Table 1, entry 5). Amongst various bases screened, Cs2CO3 and KOH afforded the symmetrical aryl sulfides in excellent yields (Table 1, entries 4, 5). Other bases such as K2CO3 and K3PO4 gave lesser amounts of the desired product (Table 1, entries 3, 6). Among the solvents, DMSO yielded the best results (Table 1, entry 5) whereas PEG and DMF gave the products in moderate yields (Table 1, entries 9 and 10), whilst solvents such as toluene and water were ineffective (Table 1, entries 7 and 8). The coupling reaction did not occur in the absence of the catalyst (Table 1, entry 11) or base (Table 1, entry 12). When the reaction was conducted either at room temperature and 80 °C, no product was obtained or the yield was very low (Table 1, entries 1 and 2). The ideal temperature for the reaction was found to be 130 °C.

A study was conducted on C–S cross-coupling reaction using various sulfur sources under these conditions (Table 2). Among these sulfur surrogates potassium thiocyanate gave good yields in this C–S cross-coupling reaction.

Table 2: Nano CuO catalyzed C–S cross-coupling of iodobenzene with different sulfur sources.a

Entry Aryl halide Sulfur source Yield (%)b
1 [Graphic 1] KSCN 94
2 NH4SCN 91
3 Na2S2O3 59
4 [Graphic 2] KSCN 91
5 NH4SCN 85
6 Na2S2O3 54
7 [Graphic 3] KSCN 92
8 NH4SCN 81
9 Na2S2O3 58

aReaction conditions: Aryl halides (2.0 mmol), sulfur sources (1.5 mmol), nano CuO (5.0 mol %), DMSO (2.0 mL), KOH (2.0 equiv), 130 °C, 20 h, bIsolated yield.

While expanding the scope of this nano CuO catalyzed tandem cross-coupling, the reaction of potassium thiocyanate with various aryl halides was examined under the optimized conditions. In general, all the reactions were very clean, and the symmetrical aryl sulfides were obtained in moderate to good yields. This protocol efficiently coupled iodobenzenes with electron donating groups (e.g., Me, OMe and Et) with potassium thiocyanate to produce the corresponding products in excellent yields (Table 3, entries 4, 6 and 8), whereas in the presence of an electron withdrawing group (CF3, NO2) a slight decrease in the yield of the diaryl sulfide (Table 3, entries 12 and 13) was observed. Under these reaction conditions, various hetero aromatic iodides were reacted with potassium thiocyanate and gave the corresponding diaryl sulfides in appreciable yields (Table 3, entries 15, 16 and 17). In case of the reactions of aromatic and hetero aromatic bromides with potassium thiocyanate, longer reaction times were required in order to obtain reasonable yields of diaryl sulfides (Table 3, entry 2, 5, 7 and 18). Iodobenzene was found to be a more reactive substrate than bromo, and chloro benzenes (Table 3, entries 1, 2 and 3).

Table 3: Copper oxide nanoparticles catalyzed synthesis of diaryl sulfidesa.

[Graphic 4]
Entry Aryl halide Product Yield (%)b
1 [Graphic 5] [Graphic 6] 94
2 [Graphic 7] [Graphic 8] 63c
3 [Graphic 9] [Graphic 10] trace
4 [Graphic 11] [Graphic 12] 91
5 [Graphic 13] [Graphic 14] 68c
6 [Graphic 15] [Graphic 16] 92
7 [Graphic 17] [Graphic 18] 70c
8 [Graphic 19] [Graphic 20] 87
9 [Graphic 21] [Graphic 22] 72
10 [Graphic 23] [Graphic 24] 78
11 [Graphic 25] [Graphic 26] 76
12 [Graphic 27] [Graphic 28] 79
13 [Graphic 29] [Graphic 30] 78
14 [Graphic 31] [Graphic 32] 75
15 [Graphic 33] [Graphic 34] 66
16 [Graphic 35] [Graphic 36] 62
17 [Graphic 37] [Graphic 38] 69
18 [Graphic 39] [Graphic 40] 72c

aReaction conditions: Aryl halides (2.0 mmol), potassium thiocyanate (1.5 mmol), nano CuO (5.0 mol %), DMSO (2.0 mL), KOH (2.0 equiv), 130 °C, 20 h. b Isolated yield. cAfter 34 h.

Conclusion

We have developed a CuO nanoparticles catalyzed synthesis of symmetrical diaryl sulfides via cascade reaction of aryl halides with potassium thiocyanate under ligand free conditions. The reaction avoids foul smelling thiols and the catalyst is economical, air stable, functions under ligand free conditions and is recyclable for up to four cycles without loss of catalytic activity [20,39-41] (Table 4).

Table 4: Copper oxide reusability of the catalyst.

Recylces Yield (%) Catalyst recovery (%)
Native 94 93
1 92 91
2 89 88
3 86 85

Experimental

General procedure for the synthesis of diaryl sulfides: A mixture of aryl iodide (2.0 mmol), potassium thiocyanate (1.5 mmol), nano CuO (5.0 mol %), and KOH (2.0 equiv) was stirred at 130 °C under a N2 atmosphere in DMSO (2.0 mL). The progress of the reaction was monitored by TLC. When the reaction was complete, the reaction mixture was allowed to cool, a 1:1 mixture ethyl acetate and water (20 mL) was added and the CuO was removed by centrifugation. The organic layer was washed successively with brine and water, and dried with Na2SO4. The solvent and volatiles were completely removed under vacuum to give the crude product, which was purified by column chromatography on silica gel to yield the analytically pure product in up to 94% yield. The identity and purity of the product was confirmed by 1H and 13C NMR spectroscopy.

Supporting Information

Supporting Information File 1: Experimental details and spectroscopic data for new compounds.
Format: PDF Size: 2.8 MB Download

Acknowledgements

KHVR and VPR thank CSIR, New Delhi, for the award of fellowship.

References

  1. Ullmann, F. Ber. Dtsch. Chem. Ges. 1903, 36, 2382.
    Return to citation in text: [1]
  2. Lindley, J. Tetrahedron 1984, 40, 1433. doi:10.1016/S0040-4020(01)91791-0
    Return to citation in text: [1]
  3. Hassan, J.; Sévignon, M.; Gozzi, C.; Schulz, E.; Lemaire, M. Chem. Rev. 2002, 102, 1359. doi:10.1021/cr000664r
    Return to citation in text: [1]
  4. Johannesson, P.; Lindeberg, G.; Johansson, A.; Nikiforovich, G. V.; Gogoll, A.; Synnergren, B.; Le Grèves, M.; Nyberg, F.; Karlén, A.; Hallberg, A. J. Med. Chem. 2002, 45, 1767. doi:10.1021/jm011063a
    Return to citation in text: [1]
  5. Mugesh, G.; Du Mont, W.-W.; Sies, H. Chem. Rev. 2001, 101, 2125. doi:10.1021/cr000426w
    Return to citation in text: [1]
  6. Morimoto, K.; Tsuji, K.; Iio, T.; Miyata, N.; Uchida, A.; Osawa, R.; Kitsutaka, H.; Takahashi, A. Carcinogenesis 1991, 12, 703. doi:10.1093/carcin/12.4.703
    Return to citation in text: [1]
  7. Sader, H. S.; Johnson, D. M.; Jones, R. N. Antimicrob. Agents Chemother. 2004, 48, 53. doi:10.1128/AAC.48.1.53-62.2004
    Return to citation in text: [1]
  8. Ceruti, M.; Balliano, G.; Rocco, F.; Milla, P.; Arpicco, S.; Cattel, L.; Viola, F. Lipids 2001, 36, 629. doi:10.1007/s11745-001-0767-8
    Return to citation in text: [1]
  9. Kaldor, S. W.; Kalish, V. J.; Davies, J. F., II; Shetty, B. V.; Fritz, J. E.; Appelt, K.; Burgess, J. A.; Campanale, K. M.; Chirgadze, N. Y.; Clawson, D. K.; Dressman, B. A.; Hatch, S. D.; Khalil, D. A.; Kosa, M. B.; Lubbehusen, P. P.; Muesing, M. A.; Patick, A. K.; Reich, S. H.; Su, K. S.; Tatlock, J. H. J. Med. Chem. 1997, 40, 3979. doi:10.1021/jm9704098
    Return to citation in text: [1]
  10. Tsutsui, H.; Hayashi, Y.; Narasaka, K. Chem. Lett. 1997, 26, 317. doi:10.1246/cl.1997.317
    Return to citation in text: [1]
  11. Uchiyama, K.; Yoshida, M.; Hayashi, Y.; Narasaka, K. Chem. Lett. 1998, 27, 607. doi:10.1246/cl.1998.607
    Return to citation in text: [1]
  12. De Martino, G.; Edler, M. C.; La Regina, G.; Coluccia, A.; Barbera, M. C.; Barrow, D.; Nicholson, R. I.; Chiosis, G.; Brancale, A.; Hamel, E.; Artico, M.; Silvestri, R. J. Med. Chem. 2006, 49, 947. doi:10.1021/jm050809s
    Return to citation in text: [1]
  13. Murata, M.; Buchwald, S. L. Tetrahedron 2004, 60, 7397. doi:10.1016/j.tet.2004.05.044
    Return to citation in text: [1]
  14. Mispelaere-Canivet, C.; Spindler, J.-F.; Perrio, S.; Beslin, P. Tetrahedron 2005, 61, 5253. doi:10.1016/j.tet.2005.03.078
    Return to citation in text: [1]
  15. Itoh, T.; Mase, T. Org. Lett. 2004, 6, 4587. doi:10.1021/ol047996t
    Return to citation in text: [1]
  16. Fernández-Rodríguez, M. A.; Shen, Q.; Hartwig, J. F. J. Am. Chem. Soc. 2006, 128, 2180. doi:10.1021/ja0580340
    Return to citation in text: [1]
  17. Lee, J.-Y.; Lee, P. H. J. Org. Chem. 2008, 73, 7413. doi:10.1021/jo801169h
    Return to citation in text: [1]
  18. Jiang, Z.; She, J.; Lina, X. Adv. Synth. Catal. 2009, 351, 2558. doi:10.1002/adsc.200900501
    Return to citation in text: [1]
  19. Taniguchi, N. J. Org. Chem. 2004, 69, 6904. doi:10.1021/jo040184q
    Return to citation in text: [1]
  20. Jammi, S.; Barua, P.; Rout, L.; Saha, P.; Punniyamurthy, T. Tetrahedron Lett. 2008, 49, 1484. doi:10.1016/j.tetlet.2007.12.118
    Return to citation in text: [1] [2]
  21. Kwong, F. Y.; Buchwald, S. L. Org. Lett. 2002, 4, 3517. doi:10.1021/ol0266673
    Return to citation in text: [1]
  22. Chen, Y.-J.; Chen, H.-H. Org. Lett. 2006, 8, 5609. doi:10.1021/ol062339h
    Return to citation in text: [1]
  23. Taniguchi, N. J. Org. Chem. 2007, 72, 1241. doi:10.1021/jo062131+
    Return to citation in text: [1]
  24. Sperotto, E.; Van Klink, G. P. M.; De Vries, J. G.; Van Koten, G. J. Org. Chem. 2008, 73, 5625. doi:10.1021/jo800491k
    Return to citation in text: [1]
  25. Rout, L.; Saha, P.; Jammi, S.; Punniyamurthy, T. Eur. J. Org. Chem. 2008, 640. doi:10.1002/ejoc.200700978
    Return to citation in text: [1]
  26. Herrero, M. T.; SanMartin, R.; Domínguez, E. Tetrahedron 2009, 65, 1500. doi:10.1016/j.tet.2008.11.062
    Return to citation in text: [1]
  27. Prasad, D. J. C.; Naidu, A. B.; Sekar, G. Tetrahedron Lett. 2009, 50, 1411. doi:10.1016/j.tetlet.2009.01.022
    Return to citation in text: [1]
  28. Wang, H.; Jiang, L.; Chen, T.; Li, Y. Eur. J. Org. Chem. 2010, 12, 2324. doi:10.1002/ejoc.201000003
    Return to citation in text: [1]
  29. She, J.; Jiang, Z.; Wang, Y. Tetrahedron Lett. 2009, 50, 593. doi:10.1016/j.tetlet.2008.11.082
    Return to citation in text: [1]
  30. Basu, B.; Mandal, B.; Das, S.; Kundu, S. Tetrahedron Lett. 2009, 50, 5523. doi:10.1016/j.tetlet.2009.07.076
    Return to citation in text: [1]
  31. Feng, Y.; Wang, H.; Sun, F.; Li, Y.; Fu, X.; Jin, K. Tetrahedron 2009, 65, 9737. doi:10.1016/j.tet.2009.09.085
    Return to citation in text: [1]
  32. Jogdand, N. R.; Shingate, B. B.; Shingare, M. S. Tetrahedron Lett. 2009, 50, 6092. doi:10.1016/j.tetlet.2009.08.064
    Return to citation in text: [1]
  33. Feng, Y.-S.; Li, Y.-Y.; Tang, L.; Wu, W.; Xu., H.-J. 2010, 51, 2489. doi:10.1016/j.tetlet.2010.02.155
    Return to citation in text: [1]
  34. Chen, C.-K.; Chen, Y.-W.; Lin, C.-H.; Lin, H.-P.; Lee, C.-F. Chem. Commun. 2010, 46, 282. doi:10.1039/b918117b
    Return to citation in text: [1]
  35. Jammi, S.; Sakthivel, S.; Rout, L.; Mukherjee, T.; Mandal, S.; Mitra, R.; Saha, P.; Punniyamurthy, T. J. Org. Chem. 2009, 74, 1971. doi:10.1021/jo8024253
    Return to citation in text: [1]
  36. Reddy, K. H. V.; Reddy, V. P.; Shankar, J.; Madhav, B.; Kumar, B. S. P. A.; Nageswar, Y. V. D. Tetrahedron Lett. 2011, 52, 2679. doi:10.1016/j.tetlet.2011.03.070
    Return to citation in text: [1]
  37. Firouzabadi, H.; Iranpoor, N.; Gholinejad, M. Adv. Synth. Catal. 2010, 352, 119–124. doi:10.1002/adsc.200900671
    Return to citation in text: [1]
  38. Correa, A.; Carril, M.; Bolm, C. Angew. Chem., Int. Ed. 2008, 47, 2880. doi:10.1002/anie.200705668
    Return to citation in text: [1]
  39. Reddy, V. P.; Swapna, K.; Kumar, A. V.; Rao, K. R. J. Org. Chem. 2009, 74, 3189. doi:10.1021/jo802731j
    Return to citation in text: [1] [2]
  40. Reddy, V. P.; Kumar, A. V.; Swapna, K.; Rao, K. R. Org. Lett. 2009, 11, 1697. doi:10.1021/ol900009a
    Return to citation in text: [1] [2]
  41. Murthy, S. N.; Madhav, B.; Reddy, V. P.; Nageswar, Y. V. D. Eur. J. Org. Chem. 2009, 34, 5902. doi:10.1002/ejoc.200900989
    Return to citation in text: [1] [2]
  42. Wong, Y.-C.; Jayanth, T. T.; Cheng, C.-H. Org. Lett. 2006, 8, 5613. doi:10.1021/ol062344l
    Return to citation in text: [1]
  43. Ke, F.; Qu, Y.; Jiang, Z.; Li, Z.; Wu, D.; Zhou, X. Org. Lett. 2011, 13, 454. doi:10.1021/ol102784c
    Return to citation in text: [1] [2] [3]
  44. Tao, C.; Lv, A.; Zhao, N.; Yang, S.; Liu, X.; Zhou, J.; Liu, W.; Zhao, J. Synlett 2011, 1, 134. doi:10.1055/s-0030-1259079
    Return to citation in text: [1] [2]
  45. Pacchioni, G. Surf. Rev. Lett. 2000, 7, 277. doi:10.1142/S0218625X00000336
    Return to citation in text: [1]
  46. Knight, W. D.; Clemenger, K.; De Heer, W. A.; Saunders, W. A.; Chou, M. Y.; Cohen, M. L. Phys. Rev. Lett. 1984, 52, 2141. doi:10.1103/PhysRevLett.52.2141
    Return to citation in text: [1] [2]
  47. Kaldor, A.; Cox, D.; Zakin, M. R. Molecular Surface Chemistry: Reactions of Gas-Phase Metal Clusters. In Adv. Chem. Phys.; Prigogine, I.; Rice, S. A., Eds.; Part 2, Vol. 70; John Wiley & Sons, Inc.: Hoboken, NJ, 1988; pp 211 ff. doi:10.1002/9780470122693.ch6
    Return to citation in text: [1] [2]
  48. Siegel, J. R.; Rosenblatt, D. H. J. Am. Chem. Soc. 1958, 80, 1753. doi:10.1021/ja01540a062
    Return to citation in text: [1]
  49. Tarbell, D. S.; Harnish, D. P. Chem. Rev. 1951, 49, 1. doi:10.1021/cr60152a001
    Return to citation in text: [1]
  50. Hoggarth, E.; Sexton, W. A. J. Chem. Soc. 1947, 815. doi:10.1039/JR9470000815
    Return to citation in text: [1]
  51. Jiang, Y.; Qin, Y.; Xie, S.; Zhang, X.; Dong, J.; Ma, D. Org. Lett. 2009, 11, 5250. doi:10.1021/ol902186d
    Return to citation in text: [1]

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