Etherification of glycerol with tert -butyl alcohol catalysed by ion-exchange resins

Klepáčová, K., Mravec, D. and Bajus, M. Etherification of glycerol with tert -butyl alcohol catalysed by ion-exchange resins Chemical Papers, Vol.60, No. 3, 2006, 224-230

Document type: Článok z časopisu / Journal Article
Collection: Chemical papers  

Author(s) Klepáčová, K.
Mravec, D.
Bajus, M.
Title Etherification of glycerol with tert -butyl alcohol catalysed by ion-exchange resins
Journal name Chemical Papers
Publication date 2006
Year available 2006
Volume number 60
Issue number 3
ISSN 0366-6352
Start page 224
End page 230
Place of publication Poland
Publisher Versita
Collection year 2006
Language english
Subject 250000 Chemical Sciences
250300 Organic Chemistry
Abstract/Summary The reaction of glycerol with tert-butyl alcohol in the liquid phase on acid Amberlyst-type ion-exchange resins was studied. The influence of temperature, mole ratio n(TBA)/n(G), water and swelling of gel, and macroreticular type of polymer catalysts on etherification reaction was investigated. The most favourable reaction temperature is 75°C. The conversion of glycerol and yield of glycerol tert-butyl ethers has increased with the mole ratio n(TBA)/n(G). Dry form of macroreticular catalysts provided the best results. Etherification reaction of glycerol with isobutylene in non-aqueous conditions gives the highest yield of desired ethers. The influence of water was studied. The gel forms of ion-exchange resins have very low catalytic activity. It can be concluded that water has an inhibition effect on ion-exchange resins. By comparing the gel and macroreticular forms of Amberlyst ion-exchange resins it can be concluded that very acid forms of macroreticular ion-exchange resins with a high degree of crosslinking are more active catalysts for the studied reaction due to their pores which are sufficiently large so that the voluminous tert-butyl ethers of glycerol can be formed. It was estimated that tert-butyl alcohol as tert-butylation agent is not suitable for etherification of glycerol with the formation of di-and triethers.
 
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