Fast aldol-Tishchenko reaction utilizing 1,3-diol monoalcoholates as the catalysts

被引:10
|
作者
Törmäkangas, OP [1 ]
Koskinen, AMP [1 ]
机构
[1] Aalto Univ, Organ Chem Lab, FIN-02015 Espoo, Finland
关键词
D O I
10.1021/op0001335
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The aldol-Tishchenko reaction of enolizable aldehydes is a simple and effective way to prepare 1,3-diol monoesters, which are widely used as coalescing agents in the paint industry. The use of monoalcoholates of 1,3-diols as catalysts gives fast and clean reactions compared with the previous use of several inorganic catalysts. The use of the proper 1,3-diol moiety in the catalyst also reduces the amount of side products which are due to ester interchange between product esters and the catalyst. The rapid water-free method developed herein allows fast preparation of monoesters with excellent yield and minimized formation of side products.
引用
收藏
页码:421 / 425
页数:5
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