Preparation of Fluoroarenes in One-Pot Diazotization and Fluoro-Dediazoniation of Aminoarenes Using HF or HF-Base. The Functions of Bases in the HF Solution
- 1 July 1990
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 63 (7) , 2058-2062
- https://doi.org/10.1246/bcsj.63.2058
Abstract
In a one-pot diazotization of anilines followed by fluoro-dediazoniation in situ using HF or HF with bases (HF-Base) as a solvent, the diazotization stage has been found to play the most important part to yield fluoroarenes effectively. Diazotization of anilines was greatly influenced by the composition of the HF solution, and greatly enhanced by employing appropriate amounts of bases, such as pyridine. On the other hand, fluorodediazoniation of diazonium salts, once formed, took place very readily in HF or HF-Base to produce fluoroarenes in high yield, although such bases served to slow down the rate of decomposition of diazonium salts to some extent.This publication has 12 references indexed in Scilit:
- Preparation of fluoroaromatics - Diazotization-fluorodediazoniation of aminoaromatics.Journal of Synthetic Organic Chemistry, Japan, 1989
- Diazotisations in Highly Concentrated Mineral Acids: The nitrosation mechanism of anilinium and hydroxylammonium ions through proton loss from the ammonio groupHelvetica Chimica Acta, 1988
- Vibrational spectra and structure of polyanilineMacromolecules, 1988
- A facile preparation of fluoropyridines from Aminopyridines via diazotization and fluorodediazoniation in HF or HF-pyridine solutionsJournal of Fluorine Chemistry, 1988
- An Improved Procedure for Diazotization Fluoro-Dediazoniation of Anilines Using Organic Base-HF AgentsSynthetic Communications, 1987
- The effect of ring substituents on the dediazotisation of aromatic diazonium fluoridesJournal of Fluorine Chemistry, 1987
- Kinetics of acid and nucleophile catalysis of the diazotization of 1-naphthylamineCanadian Journal of Chemistry, 1986
- Synthetic methods and reactions. 63. Pyridinium poly(hydrogen fluoride) (30% pyridine-70% hydrogen fluoride): a convenient reagent for organic fluorination reactionsThe Journal of Organic Chemistry, 1979
- Evidence for phenyl cation as an intermediated in reactions of benzenediazonium salts in solutionJournal of the American Chemical Society, 1975
- Synthesis of Aromatic Fluorides through Diazotization in Anhydrous Hydrogen FluorideJournal of the American Chemical Society, 1950