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Unexpected Decarbonylation of Acylethynylpyrroles under the Action of Cyanomethyl Carbanion: A Robust Access to Ethynylpyrroles.


ABSTRACT: It has been found that the addition of CH2CN- anion to the carbonyl group of acylethynylpyrroles, generated from acetonitrile and t-BuOK, results in the formation of acetylenic alcohols, which undergo unexpectedly easy (room temperature) decomposition to ethynylpyrroles and cyanomethylphenylketones (retro-Favorsky reaction). This finding allows a robust synthesis of ethynylpyrroles in up to 95% yields to be developed. Since acylethynylpyrroles became available, the strategy thus found makes ethynylpyrroles more accessible than earlier. The quantum-chemical calculations (B2PLYP/6-311G**//B3LYP/6-311G**+C-PCM/acetonitrile) confirm the thermodynamic preference of the decomposition of the intermediate acetylenic alcohols to free ethynylpyrroles rather than their potassium derivatives.

SUBMITTER: Tomilin DN 

PROVIDER: S-EPMC9919934 | biostudies-literature | 2023 Feb

REPOSITORIES: biostudies-literature

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Unexpected Decarbonylation of Acylethynylpyrroles under the Action of Cyanomethyl Carbanion: A Robust Access to Ethynylpyrroles.

Tomilin Denis N DN   Sobenina Lyubov N LN   Belogolova Alexandra M AM   Trofimov Alexander B AB   Ushakov Igor A IA   Trofimov Boris A BA  

Molecules (Basel, Switzerland) 20230201 3


It has been found that the addition of CH<sub>2</sub>CN<sup>-</sup> anion to the carbonyl group of acylethynylpyrroles, generated from acetonitrile and <i>t</i>-BuOK, results in the formation of acetylenic alcohols, which undergo unexpectedly easy (room temperature) decomposition to ethynylpyrroles and cyanomethylphenylketones (<i>retro</i>-Favorsky reaction). This finding allows a robust synthesis of ethynylpyrroles in up to 95% yields to be developed. Since acylethynylpyrroles became available  ...[more]

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