Continuous flow synthesis of alkynes from isoxazolones

The development of a continuous flow approach for the generation of alkynes from isoxazolones under diazotisation conditions is reported. The underlying transformation has been known for several decades; however, in batch mode, it is plagued by variable yields, excessive use of sodium nitrite and limited scalability due to its exothermic nature and the release of copious amounts of toxic nitroxide gases. The presented flow approach overcomes these limitations and delivers various alkyne products in residence times of less than 1 minute with productivities of <i>ca.</i> 2 g h<sup>-1</sup>. This demonstrates the value of continuous flow processing in miniaturised devices and renders this alkyne forming method an attractive addition to the limited synthetic toolbox towards this important functional group.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2024-12-20
DOI
https://doi.org/10.1039/d4ob01772b
Citations
2
Primary Topic
Innovative Microfluidic and Catalytic Techniques Innovation
Type
article
Field-Weighted Citation Impact
0.37

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article

Continuous flow synthesis of alkynes from isoxazolones

Aisling Loftus, Marcus Baumann, Rosa De Gregorio
2 citations
Organic & Biomolecular Chemistry
Innovative Microfluidic and Catalytic Techniques Innovation
0.37
article

Continuous flow synthesis of alkynes from isoxazolones

Aisling Loftus, Marcus Baumann, Rosa De Gregorio
article en
2 citations

Abstract

The development of a continuous flow approach for the generation of alkynes from isoxazolones under diazotisation conditions is reported. The underlying transformation has been known for several decades; however, in batch mode, it is plagued by variable yields, excessive use of sodium nitrite and limited scalability due to its exothermic nature and the release of copious amounts of toxic nitroxide gases. The presented flow approach overcomes these limitations and delivers various alkyne products in residence times of less than 1 minute with productivities of <i>ca.</i> 2 g h<sup>-1</sup>. This demonstrates the value of continuous flow processing in miniaturised devices and renders this alkyne forming method an attractive addition to the limited synthetic toolbox towards this important functional group.

Organic & Biomolecular ChemistryVol. 23(6)
University College Dublin (IE)
University College Dublin
Openalex Percentile: Top 41%
Innovative Microfluidic and Catalytic Techniques Innovation
0.37
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