OPTIMIZATION OF TIME REACTION AND HYDROXIDE ION CONCENTRATION ON FLAVONOID SYNTHESIS FROM BENZALDEHYDE AND ITS DERIVATIVES

https://doi.org/10.22146/ijc.21825

Sri Handayani(1*), Sunarto, Sunarto,(2), Susila Kristianingrum(3)

(1) Chemistry Education Departement, Faculty of Mathematics and Natural Sciences Yogyakarta State University, Yogyakarta
(2) Chemistry Education Departement, Faculty of Mathematics and Natural Sciences Yogyakarta State University, Yogyakarta
(3) Chemistry Education Departement, Faculty of Mathematics and Natural Sciences Yogyakarta State University, Yogyakarta
(*) Corresponding Author

Abstract


The aim of this research is to determine the optimum time of reaction and concentration of hydroxide ion on chalcone, 4-methoxychalcone and 3,4-dimethoxychalcone synthesis. Chalcone and its derivatives were synthesized by dissolving KOH in ethanol followed by dropwise addition of acetophenone and benzaldehyde. Then, the mixture was stirred for several hours. Three benzaldehydes has been used, i.e : benzaldehyde, p-anysaldehyde and veratraldehyde. The time of reaction was varied for, 12, 18, 24, 30 and 36 hours. Furthermore, on the optimum reaction time for each benzaldehyde the hydroxyl ion concentration was varied from 5,7,9,11 and 13%(w/v). The results of this research suggested that the optimum time of chalchone synthesis was 12 hours, while, 4-methoxychalcone and 3,4-dimethoxychalcone were 30 hours. The optimum concentration of hydroxide ion of chalcone synthesis was 13% and for 4-methoxychalcone and 3,4-dimethoxychalcone were 11%.


Keywords


Chalcone synthesis; time of reaction; hydroxide ion concentration

Full Text:

Full Text PDF


References

[1] Tommasi, N.D., and Pizza, C., 1997, J. Nat. Prod., 60, 270-273

[2] Orjala, J., Wright, A.D., Behrends, H. Folkers, G. and Sticher, O., 1994, J. Nat. Prod., 57,1,18

[3] Bhattacharyya, J., Batista, J.S. and Almeida, R.N., 1995, Phytochemistry, 38, 277

[4] Diedrich, D.F., 1962, J. Med. Pharm. Chem., 5, 1054

[5] Iinuma, M., Tanka, T., dan Matsuura, S., 1984 , Chem. Phar. Bull , 32 (6), 2296

[6] Alcantara, A.R., Marinas, J.M. and Sinistera, J.V., 1987, Tetrahedron Letter, 28, 1515

[7] Spearing, P., Majestich, G. and Bhattacharya, J., 1997, J. Nat. Prod., 60, 399

[8] Handayani, S., 2000, Sintesis 4’-metoksiflavanon Menggunakan O-Hidroksiasetofenon dan p-Anisaldehida dari Minyak Adas, Thesis, Pascasarjana UGM, Jogjakarta.

[9] Ismiyarto, 1998, Sintesis Senyawa Kalkon dan Flavanon Menggunakan Bahan Dasar Senyawa Turunan Asetofenon dan Benzaldehida, Thesis, Pascasarjana UGM, Jogjakarta

[10] Harborne, J.B., and Mabry, T.J., 1975, The Flavonoid, Academic Press, New York

[11] Shimokoriyama, M, 1957, J. Am. Chem. Soc., 79, 4199

[12] Harborne, J.B., and Mabry, T.J., 1982, The Flavonoid : Advanced in Research, Chapman and Hall, London

[13] Mabry, T.J., Markham, K.R. dan Thomas, M.B., 1970, The Systematic Identification of Flavonoids, Springer – Verlag, New York

[14] Markham, K.R., 1988, Cara Mengidentifikasi Flavonoid, (diterjemahkan oleh Kosasih Padmawinata), Penerbit ITB, Bandung



DOI: https://doi.org/10.22146/ijc.21825

Article Metrics

Abstract views : 2807 | views : 4928


Copyright (c) 2010 Indonesian Journal of Chemistry

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

 


Indonesian Journal of Chemistry (ISSN 1411-9420 /e-ISSN 2460-1578) - Chemistry Department, Universitas Gadjah Mada, Indonesia.

Web
Analytics View The Statistics of Indones. J. Chem.