Electrochemical fluorination (ECF), or electrofluorination, is a foundational organofluorine chemistry method for the preparation of fluorocarbon-based organofluorine compounds.[1] The general approach represents an application of electrosynthesis. The fluorinated chemical compounds produced by ECF are useful because of their distinctive solvation properties and the relative inertness of carbon–fluorine bonds. Two ECF synthesis routes are commercialized and commonly applied: the Simons process and the Phillips Petroleum process. It is also possible to electrofluorinate in various organic media.[2] Prior to the development of these methods, fluorination with fluorine, a dangerous oxidizing agent, was a dangerous and wasteful process. ECF can be cost-effective, but it may also result in low yields.

Simons process

The Simons process, named after Joseph H. Simons entails electrolysis of a solution of an organic compound in a solution of hydrogen fluoride. An individual reaction can be described as:

R3C–H + HF → R3C–F + H2

In the course of a typical synthesis, this reaction occurs once for each C–H bond in the precursor. The cell potential is maintained near 5–6 V. The anode is nickel-plated. Simons discovered the process in the 1930s at Pennsylvania State College (U.S.), under the sponsorship of the 3M Corporation.[citation needed] The results were not published until after World War II because the work was classified due to its relevance to the manufacture of uranium hexafluoride.[citation needed]

In 1949 Simons and his coworkers published a long paper in the Journal of the Electrochemical Society.[3]

The Simons process is used for the production of perfluorinated amines, ethers, carboxylic acids, and sulfonic acids. For carboxylic and sulfonic acids, the products are the corresponding acyl fluorides and sulfonyl fluorides. The method has been adapted to laboratory-scale preparations. Two noteworthy considerations are (i) the hazards associated with hydrogen fluoride (the solvent and fluorine source) and (ii) the requirement for anhydrous conditions.[4]

Phillips Petroleum process

This method is similar to the Simons Process but is typically applied to the preparation from volatile hydrocarbons and chlorohydrocarbons.[5] In this process, electrofluorination is conducted at porous graphite anodes in molten potassium fluoride in hydrogen fluoride. The species KHF2 is relatively low melting, a good electrolyte, and an effective source of fluorine. The technology is sometimes called “CAVE” for Carbon Anode Vapor Phase Electrochemical Fluorination and was widely used at manufacturing sites of the 3M Corporation. The organic compound is fed through a porous anode leading to exchange of fluorine for hydrogen but not chlorine.

Other methods

ECF has also been conducted in organic media, using for example organic salts of fluoride and acetonitrile as the solvent.[2] A typical fluoride source is (C2H5)3N:3HF. In some cases, acetonitrile is omitted, and the solvent and electrolyte are the triethylamine-HF mixture. Representative products of this method are fluorobenzene (from benzene) and 1,2-difluoroalkanes (from alkenes).[6]

References

  1. ^ G. Siegemund, W. Schwertfeger, A. Feiring, B. Smart, F. Behr, H. Vogel, B. McKusick "Fluorine Compounds, Organic" in "Ullmann’s Encyclopedia of Industrial Chemistry" 2005, Wiley-VCH, Weinheim. doi:10.1002/14356007.a11_349
  2. ^ a b Fred G. Drakesmith "Electrofluorination of Organic Compounds" Topics in Current Chemistry,Vol. 193, Springer, Berlin-Heidelberg, 1997.
  3. ^ J. H. Simons; Harland, W. J. (1949). "The Electrochemical Process for the Production of Fluorocarbons". Journal of the Electrochemical Society. 95: 47–66. doi:10.1149/1.2776735.
  4. ^ Lino Conte, GianPaolo Gambaretto (2004). "Electrochemical fluorination: state of the art and future tendences". Journal of Fluorine Chemistry. 125 (2): 139–144. doi:10.1016/j.jfluchem.2003.07.002.
  5. ^ Alsmeyer, Y. W.; Childs, W. V.; Flynn, R. M.; Moore, G. G. I.; Smeltzer, J. C. (1994). "Organofluorine Chemistry: Principles and Commercial Applications". In R. E. Banks; B. E. Smart; J. C. Tatlow (eds.). Organofluorine Chemistry. Boston, MA: Springer. pp. 121–143. doi:10.1007/978-1-4899-1202-2_5.
  6. ^ Doobary, S.; Sedikides, A.T.; Caldora, H.P.; Poole, D.L.; Lennox, A.J.J. (2019-11-07). "Electrochemical Vicinal Difluorination of Alkenes: Scalable and Amenable to Electron-Rich Substrates". Angewandte Chemie International Edition. 59 (3): 1155–1160. doi:10.1002/anie.201912119. PMC 6973232. PMID 31697872.
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