Publication | Closed Access
A Practical and Convenient Fluorination of 1,3-Dicarbonyl Compounds Using Aqueous HF in the Presence of Iodosylbenzene
60
Citations
32
References
2011
Year
Chemical Engineering1,3-Dicarbonyl CompoundsEngineeringFluorous SynthesisOrganic ChemistryConvenient FluorinationChemistryHalogenationDerivative (Chemistry)Fluorination Reaction
A simple, practical, and convenient fluorination of 1,3-dicarbonyl compounds was achieved by direct use of aqueous hydrofluoric acid and iodosylbenzene (PhIO). The reaction of ethyl benzoylacetate with the reagent system of aqueous HF and PhIO in CH(2)Cl(2) gave ethyl 2-fluoro-2-benzolyacetate in 98% yield. Other 1,3-dicarbonyl compounds including β-keto esters and 1,3-diketones underwent the fluorination reaction to give the corresponding fluorinated products in good yields.
| Year | Citations | |
|---|---|---|
2009 | 353 | |
1990 | 348 | |
1990 | 234 | |
1982 | 227 | |
1993 | 222 | |
1995 | 144 | |
2003 | 134 | |
1996 | 112 | |
1991 | 101 | |
1998 | 92 |
Page 1
Page 1