Potassium carbonate as a base for cycloalkylation of diethyl malonate and ethyl cyanoacetate in solid-liquid two phase systems

الموضوعات : Journal of the Iranian Chemical Research

Fuping Liu ¹ (School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing, China)
Yan Zhu ² (School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing, China)
Ming Lu ³ (School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing, China)

تاريخ الإرسال : 30 الأربعاء , جمادى الأولى, 1429 تاريخ التأكيد : 14 الأحد , رمضان, 1429 تاريخ الإصدار : 22 الخميس , ذو القعدة, 1429

الکلمات المفتاحية: Diethyl malonate, Ethyl cyanoacetate, Potassium carbonate, Phase transfer catalyst, Toluene,

ملخص المقالة :

The cycloalkylation of diethyl malonate and ethyl cyanoacetate with alkyl dihalide was investigated by using comminuted potassium carbonate as a base and toluene as a solvent in the presence of hexadecyltrimethylammonium bromide (HTMAB) as a phase-transfer catalyst, which provided a conventional procedure with the advantage of short reaction period and high product yield. The factors influencing the product yield and the reaction mechanism were discussed on the basis of the experimental data.

المصادر:

[1] W. Dmowski, A. Wolniewicz, J. Fluorine. Chem. 102 (2000) 141.
[2] S.Y. Nishino, EP Patent 1, 671, 937, 2006.
[3] B. Torok, A. Molnar, J. Chem. Soc., Perkin. Trans 1 (1993) 801.
[4] C.Y. Zhou, D.M. Chen, Y.Z. Jiang, Synth. Common. 17 (1987) 1377.
[5] S.M. Ma, S.H. Yin, L.T. Li, F.G. Tao, Org. Lett. 4 (2002) 505.
[6] D. Albanese, D. Landini, M.J. Penso, Org. Chem. 57 (1992) 1603.
[7] Y.R. Jorapur, J.M. Jeong, D.Y. Chi, Tetra. Lett. 47 (2006) 2435.
[8] A.T. Ben, B.Y. Le, G.R. El, M. Delmas, A.Gaset, Synth. Common. 22 (1992) 1421.
[9] M.Z. Jászay, I. Petneházy, L. Töke, B. Szajáni, Synthesis (1987) 520.
[10] W.J. Balley, J.J. Daly, J. Am. Chem. Soc. 81 (1959) 5397.
[11] R.H. Harnest, A. Burger, J. Am. Chem. Soc. 65 (1943) 370.
[12] H.R. Henze, R.L. Mckee, J. Am. Chem. Soc. 64 (1942) 1672.
[13] C. Galli, G. Illuminati, L. Mandolini, P. Tamborra, J. Am. Chem. Soc. 99 (1977) 2591.
[14] D.F. Detar, N.P. Luthra, J. Am. Chem. Soc. 102 (1980) 4505.
[15] A.D. Cort, L. Mandolini, B. Masci, J. Org. Chem. 48 (1983) 3979.
[16] H.O. Chang, J.S. Kim, H.H. Jung, J. Org. Chem. 64 (1999) 1338.