90417-47-3Relevant academic research and scientific papers
Elimination reactions of β-Cyano Thioethers: Evidence for a Carbanion Intermediate and a Change in Rate-Limiting Step
Fishbein, James C.,Jencks, William P.
, p. 5075 - 5086 (2007/10/02)
The addition reactions of thiol anions to form adducts with acrylonitrile (1), 1-chloroacrylonitrile (2), and fumaronitrile (3) and the corresponding elimination reactions were examined in aqueous solution, generally containing 8.3percent Me2SO at 25 deg C.Deuterium exchange into the methanethiol and thiosalicylate adducts of 1 is faster than elimination.Deuterium exchange causes biphasic kinetics for elimination reactions in D2O of the p-nitrothiophenol, but not of the pentafluorothiophenol, adducts 1 and 2.The kinetic solvent deuterium isotope effects of knHOH/knDOD = 2.0 for addition of thiosalicylate to form 3 and 1.1-1.2 for addition of β-mercaptoethanol and thioacetic acid anions to form 1 are smaller than the product discrimination isotope effects of kH/kD = 3.2, 2.8 and 3.2 for these reactions.These differences show that the reactions proceed through a carbanion intermediate that is protonated faster than it expels basic thiol anions.These results exclude a concerted mechanism for addition-elimination with a concurrent, separate exchange reaction.The solvent kinetic deuterium isotope effect is 3.9 for the addition of thionitrobenzoate dianion to form 3.Buffer catalysis of elimination becomes more significant with more acidic leaving groups and is larger for 3 than for 1 with a given leaving group.The results show that the rate-limiting step changes from addition-elimination of the thiol anion to proton transfer with decreasing pKa of the thiol; the same change is favored by addition of CN to the α-position for a given thiol.The effect of the α-CN group is attributed to conjugation with the developing double bond in the transition state for elimination.The Broensted slope is β = 0.90 for rate-limiting deprotonation of the pentafluorothiophenol adduct 3 and Broensted-type plots against the pKa of the leaving group have slopes of β1g = -0.25 and -0.54 for predominantly rate-limiting deprotonation and leaving group expulsion, respectively.
Pyrolysis of Sulfoxide Bearing Electron-Withdrawing Substituents on β-Position in S-Ethyl Group of Ethyl Phenyl Sulfoxide
Yoshimura, Toshiaki,Yoshizawa, Masaki,Tsukurimichi, Eiichi
, p. 2491 - 2496 (2007/10/02)
In order to obtain information concerning the reaction mechanism of the pyrolysis of a sulfoxide bearing an electron-withdrawing substituent on the β-position in the S-ethyl group of ethyl phenyl sulfoxide, 2-(substituted phenyl)ethyl aryl sulfoxides (1) and 2-cyanoethyl (substituted phenyl)sulfoxides (2) were pyrolyzed.The rate-enhancing effect of the β-phenyl group of 1 was small.The activation enthalpy and entropy of 1 were found to be 110 kJ mol-1 and -45 JK-1mol-1, respectively.Hammett plots for 1 gave positive trends for the substituents, both on the β-phenyl group (ρ=0.76) and on the S-phenyl group (ρ=0.32), though the ρ-value of the latter was about half of the former.On the other hand, the Hammett plot for 2 did not give a straight line, but a concave curve in which a series of substituents from the p-OCH3 to p-Cl groups gave a negative trend (ρ=-0.49), while the p-NO2 group afforded a positive trend.The pyrolytic rate of 2 was found to be about 23-times faster than that of 1 at 100 deg C.The kinetic isotope effect for β-position hydrogen in the β-phenylethyl group of 1 was considerably large (kH/kD=4.3).From the obtained results, it was suggested that the pyrolysis of 1 and 2 proceeds via a nearly carbanion-like mechanism in a five-membered cyclic transition state.
