Conclusions
The Ni(acac)2-Et3Al and Ni(acac)2-i-Bu3Al systems effectively catalyze with 1,4-addition of methyldichlorosilane to 1,3-dienes at 20–25‡C. In the case of butadiene and isoprene, the reaction is accompanied by the formation of appreciable amounts of bis-silylated products, viz., 1,4-bis(methyldichlorosilyl)-cis-2-butene and 1,4-bis(methyldichlorosilyl)-3-methyl-2-butene.
Similar content being viewed by others
Literature cited
K. Yamamoto, T. Hayashi, and M. Kumada, J. Organomet. Chem.,28, C 37 (1971).
V. Vaisarova, J. Landova, and J. Hetflejs, Z. Chem., 64 (1974).
J. Rejon and J. Hetflejs, Coll. Czech. Chem. Commun.,40, 3190 (1975).
M. Carka and J. Hetflejs, Coll. Czech. Chem. Commun.,40, 2073 (1975).
K. Tamao, N. Miyake, Y. Kiso, and M. Kumada, J. Am. Chem. Soc.,97, 5603 (1975).
M. F. Lappert, T. A. Nile, and S. Takachashi, J. Organomet. Chem.,72, 426 (1974).
V. P. Yur'ev, I. M. Salimgareeva, O. Zh. Zhebarov, and G. A. Tolstikov, Zh. Obshch. Khim.,46, 372 (1976).
Author information
Authors and Affiliations
Additional information
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 2, pp. 418–421, February, 1979.
Rights and permissions
About this article
Cite this article
Salimgareeva, I.M., Zhebarov, O.Z., Akhmetov, R.R. et al. Hydrosilylation of 1,3-dienes with methyldichlorosilane in the presence of Ni catalyst systems. Russ Chem Bull 28, 386–389 (1979). https://doi.org/10.1007/BF00925891
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00925891