A variety of hydrolytic mixtures for the cleavage of glycoside bonds in hesperidin was studied. The optimum system for complete hydrolysis of hesperidin to prepare the aglycone consisted of CH3COOH, H2SO4, and C2H5OH at a ratio of 1:1:9. Studies of the kinetics of the hesperidin hydrolysis reaction in this system showed that the process was a first-order reaction, as demonstrated by the constant k. The maximum aglycone yield over time, 98%, was obtained by boiling the reaction mix for 8.5 h. This confirmed the suitability of our model. Prepared of hesperidin-7-O-glucoside should be by fractional hydrolysis in a system consisting of CH3COOH, H2SO4, and C2H5OH at a ratio of 1:1:9.
Similar content being viewed by others
References
E. Middleton, Int. J. Pharmacognosy, 439, 175 – 182 (1996).
A. S. Saraf, and É. T. Oganesyan, Khim.-Farm. Zh., 25(2), 4 – 8 (1991).
D. Yu. Korul’kin, Natural Flavonoids, Siberian Branch, Russian Academy of Sciences, Novosibirsk; Geo Academic Press, Institute of Organic Chemistry, Novosibirsk (2007), pp. 191 – 220.
T. Brasseur, Pharm. Belg., 44(6), 403 – 410 (1989).
O. Benavente-Garcia, J. Castillo, F. R. Marin, et al., Agr. Food Chem., 45(12), 4506 – 4514 (1997).
B. S. G. Winkel, The Science of Flavonoids, Columbus, Ohio (2006), pp. 47 – 71.
Medicines Manufactured by Foreign Firms in Russia [in Russian], AstraFarmservis, Moscow (1993).
J. Cha and Y. Cho, Hanguk Nonghwa Hakhoechi, 40(6), 577 – 582 (1997).
I. Nouya, A. Shigery, O. Yosheshico, et al., Carbohydrates, 43(11), 1212 – 1218 (1996).
F. Smith and H. C. Srivastava, J. Amer. Chem. Soc., 78, 1404 (1956).
Author information
Authors and Affiliations
Additional information
Translated from Khimiko-Farmatsevticheskii Zhurnal, Vol. 47, No. 11, pp. 36 – 39, November, 2013.
Rights and permissions
About this article
Cite this article
Evseeva, O.S., Andreeva, O.A. & Oganesyan, É.T. Studies of the Hydrolysis of Hesperidin. Pharm Chem J 47, 606–609 (2014). https://doi.org/10.1007/s11094-014-1018-6
Received:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11094-014-1018-6