The chemistry of stable carbenes .2. Benzoin-type condensations of formaldehyde catalyzed by stable carbenes

被引:1
|
作者
Teles, JH [1 ]
Melder, JP [1 ]
Ebel, K [1 ]
Schneider, R [1 ]
Gehrer, E [1 ]
Harder, W [1 ]
Brode, S [1 ]
Enders, D [1 ]
Breuer, K [1 ]
Raabe, G [1 ]
机构
[1] RHEIN WESTFAL TH AACHEN,INST ORGAN CHEM,D-52074 AACHEN,GERMANY
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中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Stable carbenes derived from thiazole, 1H-imidazole, and 4H-1,2,4-triazole are efficient catalysts for benzoin-type condensations of formaldehyde. Catalysts derived from N-substituted thiazolium salts trimerize formaldehyde to dihydroxyacetone (II). Catalysts based on 1,4-disubstituted 4H-1,2,4-triazol-1-ium salts give glycolaldehyde (I) as the main product and no II, whereas N,N'-disubstituted 1H-imidazol-3-ium salts yield mixtures of both products. The isolation of several intermediates in the catalytic cycle provide a better insight into the reaction mechanism.
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页码:61 / 83
页数:23
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