Введення дифторо(метокси)метильної групи в ароматичне кільце та дослідження її електронних властивостей

A simple and efficient method for synthesizing aromatic compounds with a difluoro(methoxy)methyl fragment (CF2OCH3) by the fluorodesulfurization of thionoesters has been developed. Systematic screening identified SnCl4/DAST as the optimal reagent combination, providing excellent selectivity and high yields of target products. A series of aromatic difluoro(methoxy)methyl compounds was synthesized under these conditions. Further studies of the electronic properties of the difluoro(methoxy)methyl group using 19F NMR allowed us to determine its Hammett constants for inductive (σI) and resonance (σR) effects. The results show that CF2OCH3 acts as a moderately electron-withdrawing substituent, underscoring its potential as a versatile group for designing organic molecules with precisely tuned electronic characteristics.

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Journal
Scientific periodicals of Ukraine
Published
2024-12-03
Primary Topic
Fluorine in Organic Chemistry
Type
article
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article

Введення дифторо(метокси)метильної групи в ароматичне кільце та дослідження її електронних властивостей

Scientific periodicals of Ukraine
Fluorine in Organic Chemistry
article

Введення дифторо(метокси)метильної групи в ароматичне кільце та дослідження її електронних властивостей

article en

Abstract

A simple and efficient method for synthesizing aromatic compounds with a difluoro(methoxy)methyl fragment (CF2OCH3) by the fluorodesulfurization of thionoesters has been developed. Systematic screening identified SnCl4/DAST as the optimal reagent combination, providing excellent selectivity and high yields of target products. A series of aromatic difluoro(methoxy)methyl compounds was synthesized under these conditions. Further studies of the electronic properties of the difluoro(methoxy)methyl group using 19F NMR allowed us to determine its Hammett constants for inductive (σI) and resonance (σR) effects. The results show that CF2OCH3 acts as a moderately electron-withdrawing substituent, underscoring its potential as a versatile group for designing organic molecules with precisely tuned electronic characteristics.

Scientific periodicals of Ukraine
National Academy of Sciences of Ukraine (UA), Institute of Organic Chemistry (UA), Enamine (Ukraine) (UA)
Openalex Percentile: Top 57%
Fluorine in Organic Chemistry
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