Base-Free Fluoride-Mediated Vinylation of Alcohols with Calcium Carbide

Here, we demonstrate that the reaction between calcium carbide and aliphatic and benzyl alcohols does not require an additional base as a catalyst and can be effectively promoted by readily available potassium fluoride. Potassium fluoride acts as a phase-transferring reagent, activating the calcium hydroxide base released from the reaction of calcium carbide with water. Given this insight, we have developed a novel synthetic pathway for the construction of alkyl vinyl ethers.

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Publication Details

Journal
Russian Journal of General Chemistry
Published
2024-12-01
DOI
https://doi.org/10.1134/s1070363224120041
Citations
2
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.42
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article

Base-Free Fluoride-Mediated Vinylation of Alcohols with Calcium Carbide

Vladimir V. Voronin, Maria S. Ledovskaya
2 citations
Russian Journal of General Chemistry
Fluorine in Organic Chemistry
0.42
article

Base-Free Fluoride-Mediated Vinylation of Alcohols with Calcium Carbide

Vladimir V. Voronin, Maria S. Ledovskaya
article en
2 citations

Abstract

Here, we demonstrate that the reaction between calcium carbide and aliphatic and benzyl alcohols does not require an additional base as a catalyst and can be effectively promoted by readily available potassium fluoride. Potassium fluoride acts as a phase-transferring reagent, activating the calcium hydroxide base released from the reaction of calcium carbide with water. Given this insight, we have developed a novel synthetic pathway for the construction of alkyl vinyl ethers.

Russian Journal of General ChemistryVol. 94(12)
St Petersburg University (RU)
Clean water and sanitation
Openalex Percentile: Top 40%
Fluorine in Organic Chemistry
0.42
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