Phenyllithium
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| Names | |
|---|---|
| Systematic IUPAC name
Phenyllithium[2] | |
| Other names
Lithiobenzene[1]
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| Identifiers | |
3D model (JSmol)
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| Abbreviations | LiPh, PhLi |
| 506502 | |
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.008.838 |
| EC Number |
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| 2849 | |
| MeSH | phenyllithium |
PubChem CID
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|
CompTox Dashboard (EPA)
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| Properties | |
| LiC 6H 5 | |
| Molar mass | 84.045 g mol−1 |
| Appearance | Colorless crystals |
| Density | 828 mg cm−3 |
| Boiling point | 140 to 143 °C (284 to 289 °F; 413 to 416 K) |
| Reacts | |
| Thermochemistry | |
Std enthalpy of
formation (ΔfH⦵298) |
48.3-52.5 kJ mol−1 |
| Hazards | |
| GHS labelling: | |
  
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| Danger | |
| H226, H250, H261, H302, H312, H314, H332 | |
| P210, P222, P231+P232, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P280, P301+P312, P301+P330+P331, P302+P334, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P363, P370+P378, P402+P404, P403+P235, P405, P422, P501 | |
| Safety data sheet (SDS) | External MSDS |
| Related compounds | |
Related compounds
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phenylcopper, phenylsodium, phenylcobalt |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Phenyllithium is an organometallic agent with the empirical formula C6H5Li. It is most commonly used as a metalating agent in organic syntheses and a substitute for Grignard reagents for introducing phenyl groups in organic syntheses.[3] Crystalline phenyllithium is colorless; however, solutions of phenyllithium are various shades of brown or red depending on the solvent used and the impurities present in the solute.[4]
Preparation
[edit]Phenyllithium was first produced by the reaction of lithium metal with diphenylmercury:[5]
- (C6Η5)2Ηg + 2Li → 2C6Η5Li + Ηg
Reaction of a phenyl halide with lithium metal produces phenyllithium:
- X-Ph + 2Li → Ph-Li + LiX
Phenyllithium can also be synthesized with a metal-halogen exchange reaction:
- n-BuLi + X-Ph → n-BuX + Ph-Li
The predominant method of producing phenyllithium today are the latter two syntheses.
Reactions
[edit]The primary use of PhLi is to facilitate formation of carbon-carbon bonds by nucleophilic addition and substitution reactions:
- PhLi + R2C=O → PhR2COLi
2-Phenylpyridine is prepared by the reaction of phenyl lithium with pyridine, a process that entails an addition-elimination pathway:[6]
- C6H5Li + C5H5N → C6H5-C5H4N + LiH
Structure and properties
[edit]Phenyllithium is an organolithium compound that forms monoclinic crystals. Solid phenyllithium can be described as consisting of dimeric Li2Ph2 subunits. The Li atoms and the ipso carbons of the phenyl rings form a planar four-membered ring. The plane of the phenyl groups are perpendicular to the plane of this Li2C2 ring. Additional strong intermolecular bonding occurs between these phenyllithium dimers and the π-electrons of the phenyl groups in the adjacent dimers, resulting in an infinite polymeric ladder structure.[7]
In solution, it takes a variety of structures dependent on the organic solvent. In tetrahydrofuran, it equilibrates between monomer and dimer states. In ether, as it is commonly sold, phenyllithium exists as a tetramer. Four Li atoms and four ipso carbon centers occupy alternating vertices of a distorted cube. Phenyl groups are at the faces of the tetrahedron and bind to three of the nearest Li atoms.
The C–Li bond lengths are an average of 2.33 Å. An ether molecule binds to each of the Li sites through its oxygen atom. In the presence of LiBr, a byproduct of directly reacting lithium with a phenyl halide, the [(PhLi•Et2O)4] complex instead becomes [(PhLi•Et2O)3•LiBr]. The Li atom of LiBr occupies one of the lithium sites in the cubane-type cluster and Br atom sits in an adjacent carbon site.[8]
References
[edit]- ^ Typically used to describe substituted derivatives. See, e.g., Katsutoshi Kobayashi; Soichi Sato; Horn, Ernst; Naomichi Furukawa (1998), "First isolation and characterization of sulfenium cation salts stabilized by the coordination of two nitrogen atoms," Tetrahedron Letters, 39: 17, pp. 2593-2596. ISSN 0040-4039. DOI 10.1016/S0040-4039(98)00277-9.
- ^ "phenyllithium (CHEBI:51470)". Chemical Entities of Biological Interest (ChEBI). Cambridge, UK: European Bioinformatics Institute. 2009-01-22. Main. Retrieved 2013-06-01.
- ^ Wietelmann, U.; Bauer, R. J. "Lithium and Lithium Compounds". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a15_393. ISBN 978-3527306732.
- ^ Gilman, H.; Zoellner, E. A.; Selby, W. M. (1932). "An Improved Procedure for the Preparation of Organolithium Compounds". Journal of the American Chemical Society. 54 (5): 1957–1962. doi:10.1021/ja01344a033.
- ^ Green, D. P.; Zuev, D. (2008). "Phenyllithium". Encyclopedia of Reagents for Organic Synthesis. Wiley and Sons. doi:10.1002/047084289X.rp076.pub2. ISBN 978-0471936237.
- ^ Evans, J. C. W.; Allen, C. F. H. "2-Phenylpyridine" Organic Syntheses (1938), vol. 18, p. 70 doi:10.15227/orgsyn.018.0070
- ^ Dinnebier, R. E.; Behrens, U.; Olbrich, F. (1998). "Lewis Base-Free Phenyllithium: Determination of the Solid-State Structure by Synchrotron Powder Diffraction". Journal of the American Chemical Society. 120 (7): 1430–1433. doi:10.1021/ja972816e.
- ^ Hope, H.; Power, P. P. (1983). "Isolation and Crystal Structures of the Halide-Free and Halide-Rich Phenyllithium Etherate Complexes [(PhLi•Et2O)4] and [(PhLi•Et2O)3•LiBr]". Journal of the American Chemical Society. 105 (16): 5320–5324. doi:10.1021/ja00354a022.
