Fluorinated alcohols:: A new medium for selective and clean reaction

被引:482
作者
Bégué, JP [1 ]
Bonnet-Delpon, D [1 ]
Crousse, B [1 ]
机构
[1] BioCIS, Ctr Etude Pharmaceut, F-92296 Chatenay Malabry, France
关键词
hexafluoroisopropanol; trifluoroethanol; oxidation; oxirane; ring opening; cycloaddition;
D O I
10.1055/s-2003-44973
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Owing to their unique properties (high hydrogen bonding donor ability, low nucleophilicity, high ionizing power and ability to solvate water), fluorinated alcohols, hexafluoroisopropanol (HFIP) and trifluoroethanol (TFE), modify the course of reactions when they are used as solvents, allowing reactions, which usually require the use of added reagents or metal catalysts to be carried out under neutral and mild conditions. New efficient and selective processes were developed for oxidation reactions, in particular with H2O2, oxirane ring-opening, and aza-Diels-Alder reactions without any catalyst. Products were easily isolated in high yields, and the fluoroalcohols could be directly recovered from the reaction medium and reused. These processes bring an improvement from an environmental point of view, by suppression of effluents, in particular heavy metals and are particularly simple, since most of the reactions do not require any work-up.
引用
收藏
页码:18 / 29
页数:12
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