Addition of Diols to 2-Methylidene-1,4-dioxaspiro[4.5]decane

A procedure has been developed for electrophilic addition of 1,2-, 1,3-, and 1,4-diols to 4-methyli­dene-1,3-dioxolane using trifluoroacetic acid as catalyst. Conditions have been found for the predominant formation of monoadducts in 31–70% yield.

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Publication Details

Journal
Russian Journal of Organic Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1134/s1070428024602486
Primary Topic
Chemical Reaction Mechanisms
Type
article
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article

Addition of Diols to 2-Methylidene-1,4-dioxaspiro[4.5]decane

Yu. G. Borisova, А. А. Голованов, S. S. Zlotskii, S. A. Sokov et al.
Russian Journal of Organic Chemistry
Chemical Reaction Mechanisms
article

Addition of Diols to 2-Methylidene-1,4-dioxaspiro[4.5]decane

Yu. G. Borisova, А. А. Голованов, S. S. Zlotskii, S. A. Sokov, Г. З. Раскильдина
article en

Abstract

A procedure has been developed for electrophilic addition of 1,2-, 1,3-, and 1,4-diols to 4-methyli­dene-1,3-dioxolane using trifluoroacetic acid as catalyst. Conditions have been found for the predominant formation of monoadducts in 31–70% yield.

Russian Journal of Organic ChemistryVol. 61(1)
Ufa State Petroleum Technological University (RU)
Openalex Percentile: Top 95%
Chemical Reaction Mechanisms
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