French
DeutschBalz–Schiemann reaction
| Balz-Schiemann reaction | |
|---|---|
| Named after | Günther Balz Günther Schiemann |
| Reaction type | Substitution reaction |
| Identifiers | |
| Organic Chemistry Portal | balz-schiemann-reaction |
| RSC ontology ID | RXNO:0000127 |
The Balz–Schiemann reaction (also called the Schiemann reaction) is a chemical reaction in which a primary aromatic amine is transformed to an aryl fluoride via a diazonium tetrafluoroborate intermediate.[1][2][3] This reaction is a traditional route to fluorobenzene and some related derivatives,[4] including 4-fluorobenzoic acid.[5]
The reaction is conceptually similar to the Sandmeyer reaction, which converts diazonium salts to other aryl halides (ArCl, ArBr).[6] However, while the Sandmeyer reaction involves a copper reagent/catalyst and radical intermediates,[7] the thermal decomposition of the diazonium tetrafluoroborate proceeds without a promoter and is believed to generate highly unstable aryl cations (Ar+), which abstract F− from BF4− to give the fluoroarene (ArF), along with boron trifluoride and nitrogen as the byproducts.
Innovations
[edit]The traditional Balz–Schiemann reaction employs HBF4 and involves isolation of the diazonium salt. Both aspects can be profitably modified. Other counterions have been used in place of tetrafluoroborates, such as hexafluorophosphates (PF6−) and hexafluoroantimonates (SbF6−) with improved yields for some substrates.[8][9] The diazotization reaction can be effected with nitrosonium salts such as [NO]SbF6 without isolation of the diazonium intermediate.[2]
As a practical matter, the traditional Balz–Schiemann reaction consumes relatively expensive BF4- as a source of fluoride. An alternative methodology produces the fluoride salt of the diazonium compound. In this implementation, the diazotization is conducted with a solution of sodium nitrite in liquid hydrogen fluoride:[10]
- ArNH2 + 2 HF + NaNO2 → [ArN2]F + NaF + 2 H2O
- [ArN2]F → ArF + N2
History
[edit]The reaction is named after the German chemists Günther Schiemann and Günther Balz.[1]
Examples
[edit]4-Fluorotoluene is made in ~89% yield by Balz-Schiemann reaction on p-toluidine.[11] This is then used as a precursor for 4-fluorobenzaldehyde,[12]
Additional literature
[edit]- Roe A (1949). "Preparation of Aromatic Fluorine Compounds from Diazonium Fluoborates". Org. React. 5: 193. doi:10.1002/0471264180.or005.04. ISBN 0471264180.
- Becker H. G. O., Israel G. (1978). "Ionenpaareffekte bei der Photolyse und Thermolyse von Aryldiazonium-tetrafluoroboraten". J. Prakt. Chem. 321 (4): 579–586. doi:10.1002/prac.19793210410.
References
[edit]- ^ a b Balz, Günther; Schiemann, Günther (1927). "Über aromatische Fluorverbindungen, I.: Ein neues Verfahren zu ihrer Darstellung" [Aromatic fluorine compounds. I. A new method for their preparation.]. Chemische Berichte (in German). 60 (5): 1186–1190. doi:10.1002/cber.19270600539.
- ^ a b Furuya, Takeru; Klein, Johannes E. M. N.; Ritter, Tobias (2010). "C–F Bond Formation for the Synthesis of Aryl Fluorides". Synthesis. 2010 (11): 1804–1821. doi:10.1055/s-0029-1218742. PMC 2953275. PMID 20953341.
- ^ Carey, Francis A.; Sundberg, Richard J. (2007). Advanced Organic Chemistry: Part B: Reactions and Synthesis (5th ed.). New York: Springer. p. 1031. ISBN 978-0387683546.
- ^ Flood, D. T. (1943). "Fluorobenzene". Organic Syntheses; Collected Volumes, vol. 2, p. 295.
- ^ G. Schiemann; W. Winkelmüller (1943). "p-Fluorobenzoic Acid". Organic Syntheses; Collected Volumes, vol. 2, p. 299.
- ^ Swain, C. G.; Rogers, R. J. (1975). "Mechanism of formation of aryl fluorides from arenediazonium fluoborates". J. Am. Chem. Soc. 97 (4): 799–800. doi:10.1021/ja00837a019.
- ^ Carey, Francis A.; Sundberg, Richard J. (2007). Advanced Organic Chemistry: Part B: Reactions and Synthesis (5th ed.). New York: Springer. p. 1030-1031. ISBN 978-0387683546.
- ^ Rutherford, Kenneth G.; Redmond, William; Rigamonti, James (1961). "The Use of Hexafluorophosphoric Acid in the Schiemann Reaction". The Journal of Organic Chemistry. 26 (12): 5149–5152. doi:10.1021/jo01070a089.
- ^ Sellers, C.; Suschitzky, H. (1968). "The use of arenediazonium hexafluoro-antimonates and -arsenates in the preparation of aryl fluorides". Journal of the Chemical Society C: Organic: 2317–2319. doi:10.1039/J39680002317.
- ^ Siegemund, Günter; Schwertfeger, Werner; Feiring, Andrew; Smart, Bruce; Behr, Fred; Vogel, Herward; McKusick, Blaine (2000). "Fluorine Compounds, Organic". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a11_349. ISBN 3527306730.
- ^ Yu, Z., Lv, Y., Yu, C., Su, W. (March 2013). "Continuous flow reactor for Balz–Schiemann reaction: a new procedure for the preparation of aromatic fluorides". Tetrahedron Letters. 54 (10): 1261–1263. doi:10.1016/j.tetlet.2012.12.084.
- ^ Laali, K. K., Herbert, M., Cushnyr, B., Bhatt, A., Terrano, D. (2001). "Benzylic oxidation of aromatics with cerium(IV) triflate; synthetic scope and mechanistic insight". Journal of the Chemical Society, Perkin Transactions 1 (6): 578–583. doi:10.1039/b008843i.