E. Márquez, Maria M. Tosta, R. Dominguez
Jul 1, 2008
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Journal
Journal of Physical Organic Chemistry
Abstract
Triethyl orthoacetate and triethyl orthopropionate were pyrolyzed in a static system over the temperature range of 291–351°C and pressure range of 80–170 Torr. The elimination reactions of these orthoesters in seasoned vessels are homogeneous, unimolecular, and follow a first-order rate law. The reaction products are ethanol, ethylene and the corresponding ethyl ester. The Arrhenius expressions of these eliminations were found as follow: for triethyl orthoacetate, log k1 (s−1) = (13.76 ± 0.09) − (187.6 ± 1.1) kJ mol−1 (2.303 RT)−1 (r = 0.9993), and for triethyl orthopropionate, log k1 (s−1) = (13.63 ± 0.07) − (193.3 ± 1.8) kJ mol−1 (2.303 RT)−1 (r = 0.9992). A reasonable mechanism of these elimination is to consider that the COCH2CH3 bond, as Cδ+…δ− OCH2CH3 in the TS, is the rate-determining step. The nucleophilicity of the oxygen atom of OCH2CH3 may abstract the hydrogen of the adjacent CH bond for a four-membered cyclic structure to give the corresponding unsaturated ketal. The unstable ketal intermediate decomposes, in a six-membered cyclic transition state, into ethylene and the corresponding ethyl ester. Copyright © 2008 John Wiley & Sons, Ltd.