Efficient Synthesis of 2‐Arylpropionitriles Via Selective Monomethylation of Aryl Acetonitriles Using an Easy to Handle Methylation Agent

Abstract A convenient and safe methylation protocol employing quaternary ammonium salts (PhMe 3 NI) as alternative methylating agents for the selective α‐methylation of arylacetonitriles is presented. This approach allows for the selective α‐methylation of arylacetonitriles, overcoming the limitations of existing techniques, while offering a practical and sustainable solution for late‐stage functionalization in medicinal chemistry. The straightforward and safe nature of this methodology makes it particularly well‐suited for applications in drug discovery. In our report, we present a diverse set of 18 examples, achieving yields of up to 76 %.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2024-09-08
DOI
https://doi.org/10.1002/ejoc.202400693
Citations
2
Primary Topic
Chemical Reactions and Isotopes
Type
article
Field-Weighted Citation Impact
0.42

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article

Efficient Synthesis of 2‐Arylpropionitriles Via Selective Monomethylation of Aryl Acetonitriles Using an Easy to Handle Methylation Agent

Johanna Templ, Eleni Papaplioura, Michael Schnürch, Nina Wildhack
2 citations
European Journal of Organic Chemistry
Chemical Reactions and Isotopes
0.42
article

Efficient Synthesis of 2‐Arylpropionitriles Via Selective Monomethylation of Aryl Acetonitriles Using an Easy to Handle Methylation Agent

Johanna Templ, Eleni Papaplioura, Michael Schnürch, Nina Wildhack
article en
2 citations

Abstract

Abstract A convenient and safe methylation protocol employing quaternary ammonium salts (PhMe 3 NI) as alternative methylating agents for the selective α‐methylation of arylacetonitriles is presented. This approach allows for the selective α‐methylation of arylacetonitriles, overcoming the limitations of existing techniques, while offering a practical and sustainable solution for late‐stage functionalization in medicinal chemistry. The straightforward and safe nature of this methodology makes it particularly well‐suited for applications in drug discovery. In our report, we present a diverse set of 18 examples, achieving yields of up to 76 %.

European Journal of Organic ChemistryVol. 27(44)
TU Wien (AT)
European Commission, Austrian Science Fund
Openalex Percentile: Top 43%
Chemical Reactions and Isotopes
0.42
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