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In-Plane Vinylic S N 2 Substitution and Intramolecular β Elimination of β-Alkylvinyl(chloro)-λ 3 -iodanes

1998; American Chemical Society; Volume: 120; Issue: 10 Linguagem: Inglês

10.1021/ja972267c

1943-2984

Tadashi Okuyama, T Takino, Koichi Sato, Masahito Ochiai,

Porphyrin and Phthalocyanine Chemistry

The reactions of four (E)-β-alkylvinyl(phenyl)iodonium salts with chloride ion were examined in acetonitrile and in several other solvents at 25 °C. The β-methyl-, β-octyl-, and β-isopropyl-substituted iodonium salts undergo competitive bimolecular nucleophilic substitution to form the corresponding (Z)-1-chloro-1-alkene with inversion of configuration at the vinylic carbon and elimination to form the 1-alkyne. The β-tert-butyl-substituted iodonium salt affords only the products of the elimination reaction. The UV absorption spectra of the reactants show the rapid coversion of chloride and iodonium ions to an equilibrium mixture of the corresponding chloro-λ3-iodane, with an association constant of 5600−7600 mol-1 dm3. A kinetic analysis shows that most of the substitution and elimination products form from reaction of the λ3-iodane. Evidence is presented that the substitution reaction proceeds by a concerted bimolecular SN2 mechanism and that the elimination reaction proceeds by a unimolecular reaction mechanism with intramolecular transfer of the β-proton to the leaving group.