Metal-Free Hydrogenation Catalyzed by an Air-Stable Borane: Use of Solvent as a Frustrated Lewis Base

被引:95
|
作者
Scott, Daniel J. [1 ]
Fuchter, Matthew J. [1 ]
Ashley, Andrew E. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AZ, England
基金
英国工程与自然科学研究理事会;
关键词
boranes; frustrated Lewis pairs; heterocycles; hydrogenation; solvent effects; SMALL-MOLECULE ACTIVATION; B(C6F5)(3)-CATALYZED HYDROSILATION; ALKENE POLYMERIZATION; PAIRS; DIHYDROGEN; IMINES; ETHERS; THF; TETRAHYDROFURAN; REACTIVITY;
D O I
10.1002/anie.201405531
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In recent years 'frustrated Lewis pairs' (FLPs) have been shown to be effective metal-free catalysts for the hydrogenation of many unsaturated substrates. Even so, limited functional-group tolerance restricts the range of solvents in which FLP-mediated reactions can be performed, with all FLP-mediated hydrogenations reported to date carried out in non-donor hydrocarbon or chlorinated solvents. Herein we report that the bulky Lewis acids B(C6Cl5)(x)(C6F5)(3-x) (x= 0-3) are capable of heterolytic H-2 activation in the strong-donor solvent THF, in the absence of any additional Lewis base. This allows metal-free catalytic hydrogenations to be performed in donor solvent media under mild conditions; these systems are particularly effective for the hydrogenation of weakly basic substrates, including the first examples of metal-free catalytic hydrogenation of furan heterocycles. The air-stability of the most effective borane, B(C6Cl5)(C6F5)(2), makes this a practically simple reaction method.
引用
收藏
页码:10218 / 10222
页数:5
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