Kinetics of ‘initial burst’ in the solid-liquid phase-transfer catalysis. Nucleophilic substitution of 2-octyl mesylate with potassium bromide

2001 ◽  
Vol 14 (6) ◽  
pp. 343-348 ◽  
Author(s):  
S. S. Yufit ◽  
S. S. Zinovyev
Keyword(s):  
Liquid Phase ◽  
Nucleophilic Substitution ◽  
Phase Transfer Catalysis ◽  
Phase Transfer ◽  
Potassium Bromide ◽  
Initial Burst ◽  
Solid Liquid ◽  
Kinetics Of

A Selective Synthesis of Unsymmetrical 1,1'-Methylenebisdiazoles by Solid-liquid Phase Transfer Catalysis

Heterocycles ◽  
1986 ◽  
Vol 24 (8) ◽  
pp. 2233 ◽  
Author(s):  
Jos� Elguero ◽  
Sebastian Juli� ◽  
Carlos Mart地ez-Martorell
Keyword(s):  
Liquid Phase ◽  
Phase Transfer Catalysis ◽  
Phase Transfer ◽  
Selective Synthesis ◽  
Solid Liquid

Solid-liquid phase-transfer catalysis reactions without solvent; very mild conditions for .beta.-eliminations

1984 ◽  
Vol 49 (6) ◽  
pp. 1138-1140 ◽  
Author(s):  
Jean Barry ◽  
Georges Bram ◽  
Guy Decodts ◽  
Andre Loupy ◽  
Philippe Pigeon ◽  
...  
Keyword(s):  
Liquid Phase ◽  
Phase Transfer Catalysis ◽  
Phase Transfer ◽  
Mild Conditions ◽  
Solid Liquid

Esterification of 1,4-dichlorobutane with sodium formate under solid–liquid phase transfer catalysis. A kinetic study

1989 ◽  
Vol 67 (2) ◽  
pp. 245-249 ◽  
Author(s):  
Hayder A. Zahalka ◽  
Yoel Sasson
Keyword(s):  
Liquid Phase ◽  
Kinetic Study ◽  
Quaternary Ammonium ◽  
Phase Transfer Catalysis ◽  
Phase Transfer ◽  
Sodium Formate ◽  
Product Distribution ◽  
Quaternary Ammonium Salts ◽  
Ammonium Salts ◽  
Solid Liquid

Kinetic data are reported regarding the esterification of 1,4-dichlorobutane with sodium formate catalyzed by quaternary ammonium salts as a model for reactions in series, under solid–liquid phase transfer conditions. The process was found to follow a consecutive first-order mechanism of the general type A → R → S. The reactivity of the quaternary ammonium salts with regard to the counteranion was Cl− > Br− > 1− > HSO4−. The reaction rate was linearly dependent on catalyst concentration up to 12 mol% of catalyst relative to the substrate. Above this concentration the rate was constant and independent of the amount of the catalyst. The activation energy of the two consecutive steps was found to be similar (21 kcal/mol). Therefore, the product distribution (R/S) is not appreciably affected by temperature. A mechanism termed "Thin aqueous boundary layer" is suggested for nucleophilic displacement reactions under solid–liquid phase transfer conditions. Keywords: phase transfer catalysis, series reactions, kinetic study.

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