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Dinuclear manganese alkoxide complexes as catalysts for C-N bond cleavage of simple tertiary N,N-dialkylamides to give esters.

ABSTRACT: Amide bonds are stable due to the resonance between the nitrogen lone pair and the carbonyl moiety, and therefore the chemical transformation of amides, especially tertiary amides, involving C-N bond fission is considered one of the most difficult organic reactions, unavoidably requiring harsh reaction conditions and strong acids or bases. We report the catalytic C-N bond cleavage of simple tertiary N,N-dialkylamides to give corresponding esters using a catalyst system (2 mol% based on Mn atoms) of a tetranuclear manganese alkoxide, [Mn(acac)(OEt)(EtOH)]4 (1c), combined with four equivalents of 4,7-bis(dimethylamino)-1,10-phenanthroline (L1: Me2N-Phen). Regarding the reaction mechanism, we isolated a dinuclear manganese complex, [Mn(acac)(OEt)(Phen)]2 (6c), which was revealed as the catalytically active species for the esterification of tertiary amides.

SUBMITTER: Nagae H 

PROVIDER: S-EPMC6429592 | biostudies-literature | 2019 Mar

REPOSITORIES: biostudies-literature

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Dinuclear manganese alkoxide complexes as catalysts for C-N bond cleavage of simple tertiary <i>N</i>,<i>N</i>-dialkylamides to give esters.

Nagae Haruki H   Hirai Takahiro T   Kato Daiki D   Soma Shusei S   Akebi Shin-Ya SY   Mashima Kazushi K  

Chemical science 20190129 10

Amide bonds are stable due to the resonance between the nitrogen lone pair and the carbonyl moiety, and therefore the chemical transformation of amides, especially tertiary amides, involving C-N bond fission is considered one of the most difficult organic reactions, unavoidably requiring harsh reaction conditions and strong acids or bases. We report the catalytic C-N bond cleavage of simple tertiary <i>N</i>,<i>N</i>-dialkylamides to give corresponding esters using a catalyst system (2 mol% base  ...[more]