(E)-1-(Benzo[d][1,3]dioxol-5-yl)-5,6,6-trimethylhept-4-en-3-one

The title compound (1) was obtained within a project to synthesize analogs of the antiepileptic drug stiripentol. Compound 1 was synthesized by aldol addition of the lithium enolate of 4-(benzo[d][1,3]dioxol-5-yl)butan-2-one (2) to 3,3-dimethylbutan-2-one (3), followed by the dehydration of the resulting β-hydroxy-ketone under acid processing. The structure of 1 was established by 1D and 2D NMR spectroscopy and high-resolution mass spectrometry.

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Publication Details

Journal
Molbank
Published
2024-12-11
DOI
https://doi.org/10.3390/m1938
Citations
2
Primary Topic
Coordination Chemistry and Organometallics
Type
article
Field-Weighted Citation Impact
0.50

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article

(E)-1-(Benzo[d][1,3]dioxol-5-yl)-5,6,6-trimethylhept-4-en-3-one

Joaquı́n Altarejos, Sofı́a Salido, Mario Rico-Molina
2 citations
Molbank
Coordination Chemistry and Organometallics
0.50
article

(E)-1-(Benzo[d][1,3]dioxol-5-yl)-5,6,6-trimethylhept-4-en-3-one

Joaquı́n Altarejos, Sofı́a Salido, Mario Rico-Molina
article en
2 citations

Abstract

The title compound (1) was obtained within a project to synthesize analogs of the antiepileptic drug stiripentol. Compound 1 was synthesized by aldol addition of the lithium enolate of 4-(benzo[d][1,3]dioxol-5-yl)butan-2-one (2) to 3,3-dimethylbutan-2-one (3), followed by the dehydration of the resulting β-hydroxy-ketone under acid processing. The structure of 1 was established by 1D and 2D NMR spectroscopy and high-resolution mass spectrometry.

MolbankVol. 2024(4)
Universidad de Jaén (ES)
Ministerio de Ciencia e Innovación, Universidad de Jaén, Centro de Instrumentación Científico-Técnica, Universidad de Jaén, Agencia Estatal de Investigación
Openalex Percentile: Top 37%
Coordination Chemistry and Organometallics
0.50
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