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一种用于钯催化芳基氯胺化反应的高活性叶立德功能化膦

A Highly Active Ylide-Functionalized Phosphine for Palladium-Catalyzed Aminations of Aryl Chlorides.

作者信息

Weber Philip, Scherpf Thorsten, Rodstein Ilja, Lichte Dominik, Scharf Lennart T, Gooßen Lukas J, Gessner Viktoria H

机构信息

Evonik Chair of Organic Chemistry, Ruhr University Bochum, ZEMOS, Universitätsstr. 150, 44801, Bochum, Germany.

Faculty of Chemistry and Biochemistry, Chair of Inorganic Chemistry II, Ruhr University Bochum, Universitätsstr. 150, 44801, Bochum, Germany.

出版信息

Angew Chem Int Ed Engl. 2019 Mar 4;58(10):3203-3207. doi: 10.1002/anie.201810696. Epub 2019 Jan 2.

Abstract

Ylide-functionalized phosphine ligands (YPhos) were rationally designed to fit the requirements of Buchwald-Hartwig aminations at room temperature. This ligand class combines a strong electron-donating ability comparable to NHC ligands with high steric demand similar to biaryl phosphines. The active Pd species are stabilized by agostic C-H⋅⋅⋅Pd rather than by Pd-arene interactions. The practical advantage of YPhos ligands arises from their easy and scalable synthesis from widely available, inexpensive starting materials. Benchmark studies showed that YPhos-Pd complexes are superior to the best-known phosphine ligands in room-temperature aminations of aryl chlorides. The utility of the catalysts was demonstrated by the synthesis of various arylamines in high yields within short reaction times.

摘要

叶立德功能化膦配体(YPhos)经过合理设计,以满足室温下布赫瓦尔德-哈特维希胺化反应的要求。这类配体结合了与NHC配体相当的强给电子能力和与联芳基膦相似的大空间需求。活性钯物种通过agostic C-H⋅⋅⋅Pd相互作用得以稳定,而非通过钯-芳烃相互作用。YPhos配体的实际优势源于其可从广泛可得的廉价起始原料轻松且可扩展地合成。基准研究表明,在芳基氯的室温胺化反应中,YPhos-钯配合物优于最知名的膦配体。通过在短反应时间内高产率地合成各种芳胺,证明了这些催化剂的实用性。

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