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Cr(VI) Oxidation of Cholesterol—A Kinetic Study Using N-Cetylpicolinium Dichromates, A Class of Novel Phase Transfer Oxidants

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Abstract

Kinetic study of cholesterol oxidation has been studied using a series of N-cetylpicolinium dichromates (CPDC), a class of phase transfer oxidants, in acetic acid medium under first order conditions with respect to oxidant. Rate constants were calculated in the temperature range 290–300 K. The kinetics was followed spectrophotometrically; cholest-5-en-3-one is found to be the only oxidation product. Unlike the previously reported lipopathic oxidant containing cetyltrimethylammonium ions, these oxidants show a direct variation of rate with the oxidant concentration ruling out any reversed micellar organization of the oxidant molecules. From the experimental data formation of an unstable cyclic transition state followed by intra-molecular proton transfer has been proposed. Solvent isotope effect for the cholesterol oxidation (\({{{{k}_{{{\text{CHC}}{{{\text{l}}}_{3}}}}}} \mathord{\left/ {\vphantom {{{{k}_{{{\text{CHC}}{{{\text{l}}}_{3}}}}}} {{{k}_{{{\text{CDCC}}{{{\text{l}}}_{3}}}}}}}} \right. \kern-0em} {{{k}_{{{\text{CDCC}}{{{\text{l}}}_{3}}}}}}}\) = 1.52) indicated a carbon-hydrogen cleavage rather than a carbon-carbon cleavage. Variation of solvent polarity is found to impose a remarkable impact on the rate of oxidation: more polar reaction environment favours the oxidation by β-CPDC oxidant to a higher extent, compared to the other two oxidant isomers, α-CPDC and γ-CPDC.

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REFERENCES

  1. Wiberg, K.B., Oxidation in Organic Chemistry, Part A, New York: Academic Press/Wiley, 1965, p. 69.

    Google Scholar 

  2. Corey, E.J., and Boger, D.L., Tetrahedron Lett., 1978, vol. 28, p. 2461

    Article  Google Scholar 

  3. Dave, I., Sharma, V., and Banerji, K.K., J. Indian Chem. Soc., 2002, vol. 79, p. 347.

    CAS  Google Scholar 

  4. Nalawaya, N., Jain, A., and Hiran, B.L., J. Indian Chem. Soc., 2002, vol. 79, p. 587.

    Google Scholar 

  5. Medien, H.A.A., Z. Naturforsch., 2003, vol. 58b, p. 1201.

    Article  Google Scholar 

  6. Kavitha, S., Pandurangan, A., and Alphonse, I., Indian J. Chem., 2005, vol. 44A, p. 715.

    CAS  Google Scholar 

  7. Pandurangan, A., Rajkumar, G.A., Arbindoo, B., and Murugesan, V., Indian J. Chem., 1999, vol. 38B, p. 99.

    CAS  Google Scholar 

  8. Vibhute, A.Y., Patwari, S.B., Khansole, S.V., and Vibhute, Y.B., Chin. Chem. Lett., 2009, vol. 20, p. 256.

    Article  CAS  Google Scholar 

  9. Hajipour, A.R., Khazdooz, L., and Ruoho, A.E., J. Iran. Chem. Soc., 2005, vol. 2, p. 315.

    Article  CAS  Google Scholar 

  10. Mansoor, S.S., and Shafi, S.S., React. Kinet. Mech. Catal., 2010, vol. 100, p. 21.

    Google Scholar 

  11. Mamaghani, M., Shirini, F., and Parsa, F., Russ. J. Org. Chem., 2002, vol. 38, p. 1113.

    Article  CAS  Google Scholar 

  12. Mansoor, S.S., and Shafi, S.S., J. Mol. Liq., 2010, vol. 155, p. 85; Mansoor, S.S., E.-J. Chem., 2011, vol. 8, no. 2, p. 643.

    Article  Google Scholar 

  13. Mansoor, S.S., and Shafi, S.S., React. Kinet. Mech. Catal., 2010, vol. 100, p. 21.

    Google Scholar 

  14. Mansoor, S.S., and Shafi, S.S., Arabian J. Chem., 2010, vol. 7, p. 171.

    Article  CAS  Google Scholar 

  15. Mansoor, S.S., and Shafi, S.S., J. Mol. Liq., 2010, vol. 155, p. 85.

    Article  CAS  Google Scholar 

  16. Starks, C.M., and Owens, R.M., J. Am. Chem. Soc., 1973, vol. 95, p. 3613.

    Article  CAS  Google Scholar 

  17. Dash, S., and Mishra, B.K., Int. J. Chem. Kinet., 1995, vol. 27, p. 627.

    Article  CAS  Google Scholar 

  18. Dash, S., and Mishra, B.K., Bull. Chem. Soc. Jpn., 1994, vol. 67, p. 3289.

    Article  CAS  Google Scholar 

  19. Dash, S., and Mishra, B.K., Indian J. Chem., 1997, vol. 36A, p. 662.

    CAS  Google Scholar 

  20. Dash, S., Nayak, B.B., and Mishra, B.K., Indian J. Chem., 2001, vol. 159, p. 40.

    Google Scholar 

  21. Nayak, B., Panigrahi, B.M., Patel, S., Dash S., and Mishra, B.K., Indian J. Chem., 2006, vol. 45A, p. 2229.

    CAS  Google Scholar 

  22. Nayak, B.B., Sahu, S., Patel, S., Dash, S., and Mishra, B.K., Indian J. Chem., 2008, vol. 47A, p. 1486.

    CAS  Google Scholar 

  23. Bank, S.P., Guru, P.S., and Dash, S., Carbohydr. Polym., 2014, vol. 111, p. 806.

    Article  CAS  PubMed  Google Scholar 

  24. Bank, S.P., Guru, P.S., and Dash, S., Spectrochim. Acta, Part A, 2015, vol. 142, p. 34.

    Article  CAS  Google Scholar 

  25. Bank, S.P., Guru, P.S., and Dash, S., Ind. Eng. Chem. Res., 2015, vol. 54, p. 9142.

    Article  CAS  Google Scholar 

  26. Priyadarshini, S., Guru, P.S., and Dash, S., Carbohydr. Polym., 2017, vol. 171, p. 122.

    Article  CAS  PubMed  Google Scholar 

  27. Dauben, W.G., Lorber, M.E., and Fullerton, D.S., J. Org. Chem., 1969, vol. 34, p. 3587.

    Article  CAS  Google Scholar 

  28. Fousteris, M.A., Koutsourea, A.I., Nikolaropoulos, S.S., Riahi, A., and Muzart, J., J. Mol. Catal. A: Chem., 2006, vol. 250, p. 70.

    Article  CAS  Google Scholar 

  29. Pearson, A.J., Chen, Y.S., Han, G.R., Hsu, S.Y., and Ray, T., J. Chem. Soc. Perkin Trans., 1985, vol. 1, p. 267.

    Article  Google Scholar 

  30. Dong, J., Chen, W., Wang, S., Zhang, J., Li, H., Guo, H., Man, Y., and Chen, B., J. Chromatography B, 2007, vol. 858, p. 239.

    Article  CAS  Google Scholar 

  31. Hector, M., Hartmannn, R.W., and Njar, V.C.O., Synth. Commun., 1996, vol. 26, p. 1075.

    Article  CAS  Google Scholar 

  32. Nangia, A., and Anthony, A., Synth. Commun., 1996, vol. 26, p. 225.

    Article  CAS  Google Scholar 

  33. Li, S., and Li, T., Steroids, 1998, vol. 63, p. 76.

    Article  CAS  PubMed  Google Scholar 

  34. Silva, M.R., Beja, A.M., and Paixao, J.A., Powder Diffr., 2003, vol. 18, p. 306.

    Article  CAS  Google Scholar 

  35. Hunter, A.C., and Priest, S., Steroids, 2006, vol. 71, p. 30.

    Article  CAS  PubMed  Google Scholar 

  36. Patel, S., and Mishra, B.K., J. Org. Chem., 2006, vol. 71, p. 3522.

    Article  CAS  PubMed  Google Scholar 

  37. Chidambaram, M., Sonavane, S.U., de la Zerda, J., and Sasson, Y., Tetrahedron, 2007, vol. 63, p. 7696.

    Article  CAS  Google Scholar 

  38. Patel, S., and Mishra, B.K., J. Org. Chem., 2006, vol. 71, p. 6759.

    Article  CAS  PubMed  Google Scholar 

  39. Bhuvaneshwari, D.S., Elango, K.P., Int. J. Chem. Kinet., 2006, vol. 38, p. 657.

    Article  CAS  Google Scholar 

  40. Hegde, R.N., Shetti, N.P., Nandibewoor, S.T., Ind. Eng. Chem. Res. 2009, vol. 48, p. 7025.

    Article  CAS  Google Scholar 

  41. Kabilan, S., Girija, R., Reis, J.C.R., Segurado, M.A.P., and Gomes de Oliveira, J.D., J. Chem. Soc., Perkin Trans. 2, 2002, p. 1151.

  42. Mansoor, S.S., Malik, V.S., Aswin, K., Logaiya, K., and Hussain, A.M., J. Saudi Chem. Soc., 2016, vol. 20, p. 77.

    Article  CAS  Google Scholar 

  43. Cotton, F.A., Wilkinson, G. Murillo, C.A., and Bochmann, M., Advanced Inorganic Chemistry, 6th ed., New York: John Wiley and Sons, 1999, vol. 747.

    Google Scholar 

  44. Brandstrom, A., Adv. Phys. Org. Chem., 1978, vol. 15, p. 267.

    Google Scholar 

  45. Glasstone, S., Laidler, K.J., and Erying, H., The Theory of Rate Process, New York: McGraw-Hill, 1941, Chapters III and IV.

  46. Zolotov, B., Gan, A., Feinberg, B.D., and Huppert, D., Chem. Phys. Lett., 1997, vol. 265, p. 418.

    Article  CAS  Google Scholar 

  47. Castner, E.W., Chang, Y.J., Chu, Y.C., and Walfaren, G.E., J. Chem. Phys., 1995, vol. 102, p. 653.

    Article  CAS  Google Scholar 

  48. Pant, D., and Levinger, N.E., J. Phys. Chem., 1999, vol. 103, p. 7846.

    Article  CAS  Google Scholar 

  49. Shirota, H., Pal, H., Tominaga, K., and Yosihara, K., J. Phys. Chem., 1996, vol. 100, p. 14575.

    Article  CAS  Google Scholar 

  50. Reid, P.J., and Barabara, P.F., J. Phys. Chem., 1995, vol. 99, p. 3554.

    Article  CAS  Google Scholar 

  51. Shirota, H., Tamato, Y., and Segawa, H., J. Phys. Chem. A, 2004, vol. 108, p. 3244.

    Article  CAS  Google Scholar 

  52. Das, S., Datta, A., and Bhattacharyya, K., J. Phys. Chem. A, 1997, vol. 101, p. 3299.

    Article  CAS  Google Scholar 

  53. Kaatze, U., Chem. Phys. Lett., 1993, vol. 203, p. 1.

    Article  CAS  Google Scholar 

  54. Marcus, Y., Wiley Series in Solution Chemistry, 1998, vol. 4.

    Google Scholar 

Download references

ACKNOWLEDGMENTS

S. Dash acknowledges the financial help extended by All India Council of Technical Education (AICTE), New Delhi, through a RPS project to set up the laboratory.

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Priyadarshini, S., Guru, P.S., DS, R. et al. Cr(VI) Oxidation of Cholesterol—A Kinetic Study Using N-Cetylpicolinium Dichromates, A Class of Novel Phase Transfer Oxidants. Kinet Catal 60, 147–154 (2019). https://doi.org/10.1134/S0023158419020083

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  • DOI: https://doi.org/10.1134/S0023158419020083

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