(Z)-1-(3,5-Dichloro-2H-pyrrol-2-ylidene)-N,N-dimethylmethanamine

The Vilsmeier–Haack reaction is a convenient method for the formylation of electron-rich aromatic compounds. However, this interaction sometimes gives specific side products. We report the isolation and structural characterization of a novel compound (Z)-1-(3,5-dichloro-2-pyrrolylidene)-N,N-dimethylmethanamine obtained as a side product during the formylation of 2-chloropyrrole. The product was characterized using NMR spectroscopy and X-ray crystallography.

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Publication Details

Journal
Molbank
Published
2025-03-11
DOI
https://doi.org/10.3390/m1979
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
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article

(Z)-1-(3,5-Dichloro-2H-pyrrol-2-ylidene)-N,N-dimethylmethanamine

Aleksey Yu. Vorob’ev, Alina A. Sonina, Daniil Rykunov
Molbank
Synthesis and biological activity
article

(Z)-1-(3,5-Dichloro-2H-pyrrol-2-ylidene)-N,N-dimethylmethanamine

Aleksey Yu. Vorob’ev, Alina A. Sonina, Daniil Rykunov
article en

Abstract

The Vilsmeier–Haack reaction is a convenient method for the formylation of electron-rich aromatic compounds. However, this interaction sometimes gives specific side products. We report the isolation and structural characterization of a novel compound (Z)-1-(3,5-dichloro-2-pyrrolylidene)-N,N-dimethylmethanamine obtained as a side product during the formylation of 2-chloropyrrole. The product was characterized using NMR spectroscopy and X-ray crystallography.

MolbankVol. 2025(1)
Novosibirsk Institute of Organic Chemistry (RU)
Openalex Percentile: Top 97%
Synthesis and biological activity
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