Abstract
Perfluoromethyldecalin solutions of the fluorous alkyl halides R f 8(CH 2) m X ( m=2, 3; X=Cl, I) are inert toward aqueous NaCl, KI, KCN, and NaOAc. However, substitution occurs at 100 °C in the presence of 10 mol % of the fluorous ammonium salts ( R f 8(CH 2) 2)(R f8 (CH 2) 5) 3N + I − ( 1) or ( R f 8(CH 2) 3) 4N + Br − ( 2) (10 mol %), which are fully or partially soluble in perfluoromethyldecalin under these conditions. Stoichiometric reactions of (a) 1 and R f 8(CH 2) 3Br, and (b) 2 and R f 8(CH 2) 2I are conducted in perfluoromethyldecalin at 100 °C, and yield the same R f 8(CH 2) m I/ R f 8(CH 2) m Br equilibrium ratio (60–65:40–35). This shows that ionic displacements can take place in extremely nonpolar fluorous phases, and suggests a classical phase transfer mechanism for the catalyzed reactions. Interestingly, the non-fluorous ammonium salt mixture CH 3(CH 3(CH 2) m ) 3N + Cl − ( 3, Aliquat ® 336; m=2:1 7/9) also catalyzes halide substitutions, but under triphasic conditions with 3 suspended between the lower fluorous and upper aqueous layers. NMR experiments establish very low solubilities in both phases, suggesting interfacial catalysis.
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