Abstract
Generalization of data on the reaction rate of catalyzed process between mercaptans and phenyl isocyanate in various media led to the conclusion that the reaction rate increased due to the specific, especially nucleophilic, solvation. The primary reaction stage is the formation of a complex between the acidic mercaptan and a base, a catalyst (triethylamine) or basic solvent.
Similar content being viewed by others
References
Dyer, E. and Glenn, J.F., J. Am. Chem. Soc., 1957, vol. 79, p. 366.
Dyer, E., Glenn, J.F., and Lendrat, E.G., J. Am. Chem. Soc., 1961, vol. 26, p. 2919.
Iwakura, J. and Okada, H., Canad. J. Chem., 1960, vol. 38, p. 2418.
Iwakura, J. and Okada, H., Canad. J. Chem. 1963, vol. 41, p. 1846.
Makitra, R.G., Midyana, G.G., Pal’chikova, E.Ya., and Romanyuk, A.V., Russ. J. Org. Chem., 2012, vol. 48, p. 25.
Koppel I.A. and Palm V.A., Adv. Linear Free Energy Relationships, Chapman, N.B. and Shorter, J., Eds., New York: Plenum Press, 1972, p. 265.
Reichardt, Ch. and Welton, T., Solvents and Solvent Effects in Organic Chemistry. Weinheim: Wiley VCH, 2011, 692.
Makitra, R.G., Turovsky, A.A., and Zaikov, G.E., Correlation Analysis in Chemistry of Solutions, Utrecht-Boston: VST. 2004, p. 22.
Recommendations for reporting the results of correlation analysis in chemistry using regression analysis. Quant. Struct. — Act. Relat., 1985, 4 no. 1, p. 29.
Author information
Authors and Affiliations
Corresponding author
Additional information
Original English Text © G.G. Midyana, R.G. Makitra, E.Ya. Pal’chikova, 2014, published in Zhurnal Organicheskoi Khimii, 2014, Vol. 50, No. 2, pp. 177–179.
Rights and permissions
About this article
Cite this article
Midyana, G.G., Makitra, R.G. & Pal’chikova, E.Y. Effect of solvent properties on reaction of isocyanates with mercaptans. Russ J Org Chem 50, 165–167 (2014). https://doi.org/10.1134/S1070428014020031
Received:
Published:
Issue Date:
DOI: https://doi.org/10.1134/S1070428014020031