Halogen Exchange in Near-Critical Water
Abdulrahman M. Alhazmi, Pia R. Alburquerque, Thomas Junk
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DOI: 10.4236/gsc.2011.14021   PDF    HTML     5,177 Downloads   9,519 Views  

Abstract

Bromoaromatics are ubiquitous in chemistry, and their manufacture is often wasteful. Halogen exchange under hydrothermal conditions constitutes a viable alternative for their synthesis in some cases. The prepara-tion of 1,2-dibromobenzene and 1-bromo-2-chlorobenzene from 1,2-dichlorobenzene, by treatment with hy-drobromic acid in hydrothermal media at temperatures ranging from 240?C to 320?C was investigated as a viable alternative to de novo synthesis. The effects of temperature, exchange duration and the presence of Fe3+ salts on product yields are discussed. Yields for both targeted haloarenes of up to 37% and 48%, respec-tively, were achieved, with very limited formation of 1,3- and 1,4-dihalobenzene isomers. A mechanism for halogen exchange was proposed.

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A. Alhazmi, P. Alburquerque and T. Junk, "Halogen Exchange in Near-Critical Water," Green and Sustainable Chemistry, Vol. 1 No. 4, 2011, pp. 128-131. doi: 10.4236/gsc.2011.14021.

Conflicts of Interest

The authors declare no conflicts of interest.

References

[1] T. Junk and W. J. Catallo, “Preparative Supercritical Deuterium Exchange in Arenes and Heteroarenes,” Tetrahedron Letters, Vol. 37, No. 20, 1996, pp. 3445-3448. doi:10.1016/0040-4039(96)00615-6
[2] M. Rossberg, W. Lendle, G. Pfleiderer, A. T?gel, E.-L. Dreher, E. Langer, H. Jaerts, P. Kleinschmidt, H. Strack, R. Cook, U. Beck, K.-A. Lipper, T. R. Torkelson, E. L?ser and K. K. Beutel, “Chlorinated Hydrocarbons,” Ullmann’s Encyclopedia of Industrial Chemistry, Wiley-VCH, Wein- heim, 2006. doi:10.1002/14356007.a06_233. pub2
[3] J. F. Hartwig, “Organotransition Metal Chemistry. From Bonding to Catalysis,” University Science Books, New York, 2010.
[4] R. Huisgen and J. Sauer, “Nucleophile Aromatische Substitution über Arine,” Angewandte Chemie, Vol. 72, No. 2, 1960, pp. 91-108. doi:10.1002/ange.19600720302
[5] “Chemical Sources USA,” Annual Edition, Chemical Sources International, Inc., Clemson, 1824.
[6] R. G. Pews and J. A. Gall, “Aromatic Fluorine Chemistry. Part 4. Preparation of 2,6-Difluoroaniline,” Journal of Fluorine Chemistry, Vol. 52, No. 3, 1991, pp. 307-316. doi:10.1016/S0022-1139(00)80345-0
[7] J. H. Clark, C. W. Jones, C. V. Duke and J. M. Miller, “Halogen Exchange Reactions of Aryl Halides Using Supported Copper (I),” Journal of Chemical Research Synopses, Vol. 8, 1989, pp. 1-238.
[8] M. N. Glukhovtsev, R. D. Bach and S. Laitner, “Single- Step and Multistep Mechanisms of Aromatic Nucleo- philic Substitution of Halobenzenes and Halonitrobenzenes with Halide Anions: Ab Initio Computational Stu- dy,” Journal of Organic Chemistry, Vol. 62, No. 12, 1997, pp.4036-4046. doi:10.1021/jo962096e
[9] Gaussian 03, Revision E.01, M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, J. A. Montgomery Jr., T. Vreven, K. N. Kudin, J. C. Burant, J. M. Millam, S. S. Iyengar, J. Tomasi, V. Barone, B. Mennucci, M. Cossi, G. Scalmani, N. Rega, G. A. Petersson, H. Nakatsuji, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, M. Klene, X. Li, J. E. Knox, H. P. Hratchian, J. B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gom
[10] A. D. Becke, “Density-Functional Thermochemistry. III. The Role of Exact Exchange,” Journal of Chemical Physics, Vol. 98, No. 7, 1993, pp. 5648-5652. doi:10.1063/1.464913
[11] C. Lee, W. Yang and R. G. Parr, “LYP Gradient-Co- rrected Functional,” Physical Review B, Vol. 37, No. 2, 1988, pp. 785-789. doi:10.1103/PhysRevB.37.785
[12] R. Lindh, A. Bernhardsson and M. Schütz, “Benzyne Thermochemistry: A Benchmark Ab Initio Study,” Journal of Physical Chemistry A, Vol. 103, No. 48, 1999, pp. 9913-9920. doi:10.1021/jp991919b
[13] S. Terabe, K. Otsuka, A. Tsuchiya and T. Ando, “Electrokinetic Separations with Micellar Solutions and Open- Tubular Capillaries,” Analytical Chemistry, Vol. 56, No. 1, 1984, pp. 111-113. doi:10.1021/ac00265a031
[14] A. T. Bottini and J. D. Roberts, “Mechanism for Liquid Phase Hydrolyses of Chlorobenzenes and Halotoluenes,” Journal of the American Chemical Society, Vol. 79, 1957, pp. 1458-1462. doi:10.1021/ja01563a050

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