Co(II) PCP Pincer Complexes as Catalysts for the Alkylation of Aromatic Amines with Primary Alcohols

Efficient alkylations of amines by alcohols catalyzed by well-defined Co­(II) complexes are described that are stabilized by a PCP ligand (N,N′-bis­(diisopropylphosphino)-N,N′-dimethyl-1,3-diaminobenzene) based on the 1,3-diaminobenzene scaffold. This reaction is an environmentally benign process im...

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Veröffentlicht in:Organic letters 2016-07, Vol.18 (14), p.3462-3465
Hauptverfasser: Mastalir, Matthias, Tomsu, Gerald, Pittenauer, Ernst, Allmaier, Günter, Kirchner, Karl
Format: Artikel
Sprache:eng
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Zusammenfassung:Efficient alkylations of amines by alcohols catalyzed by well-defined Co­(II) complexes are described that are stabilized by a PCP ligand (N,N′-bis­(diisopropylphosphino)-N,N′-dimethyl-1,3-diaminobenzene) based on the 1,3-diaminobenzene scaffold. This reaction is an environmentally benign process implementing inexpensive, earth-abundant nonprecious metal catalysts and is based on the acceptorless alcohol dehydrogenation concept. A range of primary alcohols and aromatic amines were efficiently converted into mono-N-alkylated amines in good to excellent isolated yields.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.6b01647