Dimensiosolvatic Effects. VI. Rates of Ionization of 2-Fluoro-4,4,5,5-tetramethyl-1,3-dioxolane: Dimensiosolvatic vs. Hydrogen-Bond Effects

• Published in: Bulletin of the Chemical Society of Japan 1999-06, Vol.72 (6), p.1343-1349
• Main Authors: Oki, Michinori, Ikeda, Hiroshi, Toyota, Shinji
• Format: Article
• Language: English
• ISSN: 0009-2673; 1348-0634
• DOI: 10.1246/bcsj.72.1343

The title compound was prepared by treating 4,4,5,5-tetramethyl-1,3-dioxolan-2-yl acetate with cesium fluoride. Rates of ionization of this compound were determined in various solvents by the dynamic NMR technique. While effects due to polarity as well as solvent molecular size were observed in many solvents examined, the rates in solutions of which the solvent is capable of being an acceptor in hydrogen-bond formation with the substrate were unusually small, and this effect is diminished in bulky solvents. Such results are attributed to stabilization of the original state due to hydrogen-bond formation with the acidic C(2) – H group of the substrate in those solvents. The hydrogen-bond formation is hindered by the steric effects in bulkier solvents than in smaller solvents. The rates of contact ion pair and solvent-separated ion pair formations should be independently determined in 2-fluoro-4,4,5,5-tetramethyl-1,3-dioxolane, but so far no clear example which shows that the rate-limiting step is the solvent intervention has been found, even though various bulky solvents were examined.