SYNTHESIS OF THIOMETHYLATED CALIX[4]RESORCINARENE BASED ON FENNEL OIL VIA CHLOROMETHYLATION

https://doi.org/10.22146/ijc.21411

Suryadi Budi Utomo(1*), Jumina Jumina(2), Dwi Siswanta(3), Mustofa Mustofa(4), Naresh Kumar(5)

(1) Chemical Education Study Program, PMIPA FKIP, Sebelas Maret University, Surakarta
(2) Chemistry Department, Faculty of Mathematics and Natural Sciences, Universitas Gadjah Mada, Yogyakarta
(3) Chemistry Department, Faculty of Mathematics and Natural Sciences, Universitas Gadjah Mada, Yogyakarta
(4) Department of Pharmacology and Toxicology, Faculty of Medicine, Universitas Gadjah Mada, Yogyakarta
(5) School of Chemistry, Faculty of Science, University of New South Wales, Sydney, NSW 2052
(*) Corresponding Author

Abstract


A research has been conducted to synthesize thiomethylated-C-4-methoxyphenylcalix[4]resorcinarene using fennel oil as a starting material. The synthesis was carried out in four steps i.e. (1) oxidation of anethole to yield p-anisaldehyde, (2) HCl-catalyzed condensation of p-anisaldehyde with resorcinol, (3) chloromethylation of C-4-methoxyphenylcalix[4]resorcinarene with paraformaldehyde and HCl in the presence of ZnCl2 to yield tetrakis-chloromethyl-C-4-methoxyphenylcalix[4]resorcinarene, and (4) reaction of tetrakis-chloromethyl-C-4-methoxyphenylcalix[4]resorcinarene with thiourea followed by hydrolysis with sodium hydroxide solution to yield tetrakis-thiomethyl-C-4-methoxyphenylcalix[4]resorcinarene. The prepared compounds were characterized based on melting point, FT-IR, and NMR spectrometers. According to the analysis of 1H-NMR spectrometer, C-4-methoxyphenylcalix[4]resorcinarene and tetrakis-chloromethyl-C-4-methoxyphenylcalix[4]resorcinarene were observed in the chair or flattened partial cone conformation, while tetrakis-thiomethyl-C-4-methoxyphenylcalix[4]resorcinarene tend to exist in the crown or cone conformation.

Keywords


fennel oil; chloromethylation; tetrakis-thiomethyl-C-4-methoxyphenylcalix[4]resorcinarene; flattened partial cone; crown

Full Text:

Full Text PDF


References

[1] Ketaren, S., 1990, Essential Oils, 2nd ed., Universitas Indonesia, Jakarta.

[2] Bohmer, V., 1995, Angew. Chem. Int. Ed., 34, 7, 713–745.

[3] Arora, V., Chawla, H.M., and Singh, S.P., 2007, Arkivoc, 2, 172–200.

[4] Puddephatt, R.J., 2006, Can. J. Chem., 84, 11, 1505–1514

[5] Fox, O.D., Cookson, J., Wilkinson, E.J.S., Drew, M.G.B.; MacLean, E.J., Teat, S.J., and Beer, P.D., 2006, J. Am. Chem. Soc., 128, 21, 6990–7002.

[6] Eisler, D.J., and Puddephatt, R.J., 2006, Inorg. Chem., 45, 18, 7295–7305.

[7] Jumina, Sarjono, R.E., Paramita, B.W., Siswanta, D., Santosa, S.J., Anwar, C., Sastrohamidjojo, H., Ohto, K., and Oshima, T., 2007, J. Chin. Chem. Soc., 54, 5, 1167–1178.

[8] Utomo, S.B., Jumina, and Wahyuningsih, T.D., 2009, Indo. J. Chem., 9, 3, 437–444.

[9] Moore, S.S., Tarnowski, T.L., Newcomb, M., and Cram, D.J., 1977, J. Am. Chem. Soc., 99, 19, 6398–6405.

[10] Zhao, J., Bolte, M., Dordea, C., Gruner, B., and Bohmer, V., 2009, Synthesis, 23, 4063–4067.

[11] Kalenius, E., Kekalainen, T., Neitola, R., Beyeh, K., Rissanen, K., and Vainiotalo, P., 2008, Chem. Eur. J., 14, 17, 5220–5228.

[12] Aoyoma, Y., Tanaka, Y., and Sugahara, S., 1989, J. Am. Chem. Soc., 111, 14, 5397–5404.

[13] Boas, U., and Heegaard, P.M.H., 2004, Chem. Soc. Rev., 33, 1, 43–63.

[14] Tunstand, L.M., Tucker, J.A., Dalcanale, E., Weiser, J., Bryant, J.A., Sherman, J.C., Helgeson, R.C., Knobler, C.B., and Cram, D.J., 1989, J. Org. Chem., 54, 1305–1312.

[15] Cram, D. J., Karbach, S., Kim, H.E., Knobler, C. B., Maverick, E. F., Ericson, J. L., and Helgeson, R. C., 1988, J. Am. Chem. Soc., 110, 2229

[16] Weinelt, F., and Schneider, H.-J., 1991, J. Org. Chem., 56, 19, 5527–5535.

[17] Egberink, R.J.M., Cobben, P.UH.M., Verboom, W., Harkema, S., and Reinhoudt, D.N., 1992, J. Inclusion Phenom. Mol. Recognit. Chem., 12, 1-4, 151–158.

[18] Timmerman, P., Verboom, W., and Reinhoudt, D.N., 1996, Tetrahedron, 52, 8, 2663–2704.

[19] Almi, M., Arduini, A., Casnati, A., Pochini, A., and Ungaro, R., 1989, Tetrahedron, 45, 7, 2177–2182.

[20] Hogberg, A.G.S., 1980, J. Am. Chem. Soc., 102, 6046–6050.

[21] Erdtman, H., Hoegberg, S., Abrahamsson, S., and Nilsson, B., 1968, Tetrahedron Lett., 1679

[22] Gutsche, C.D., 1989, Calixarenes. Monograph in Supramolecular Chemistry, Royal Society of Chemistry, Cambridge.



DOI: https://doi.org/10.22146/ijc.21411

Article Metrics

Abstract views : 1752 | views : 3429


Copyright (c) 2011 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.