Journal of Organic Chemistry p. 5088 - 5092 (1985)
Update date:2022-08-23
Topics:
Halpern, Marc
Zahalka, Hayder A.
Sasson, Yoel
Rabinovitz, Mordecai
Elimination of HCl and HBr from (1- and (2-haloethyl)benzenes in the presence of aqueous sodium hydroxide and quaternary ammonium salts which cannot extract hydroxide anion to the organic phase is shown to proceed via a reverse phase transfer process.The catalyst QX promotes the elimination and forms QX-HX adduct which is neutralized at the interphase by the hydroxide base.First-order kinetics is observed under conditions in which the catalyst is stable.Complicated kinetics is obtained when decomposition of the catalyst takes place simultaneously with the reaction.
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