Phenyllithium or lithobenzene 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.[2] 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.[3]

Kekulé, skeletal formula of phenyllithium
Systematic IUPAC name
Other names
Lithiobenzene[citation needed]
  • 591-51-5 checkY
3D model (JSmol)
  • Interactive image
Abbreviations LiPh, PhLi
  • CHEBI:51470 checkY
  • 10254416 checkY
ECHA InfoCard 100.008.838 Edit this at Wikidata
EC Number
  • 209-720-1
MeSH phenyllithium
  • 637932
  • DTXSID70938503 DTXSID20883453, DTXSID70938503 Edit this at Wikidata
  • InChI=1S/C6H5.Li/c1-2-4-6-5-3-1;/h1-5H; ☒N
  • [Li]c1ccccc1
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)
48.3-52.5 kJ mol−1
GHS labelling:
GHS02: FlammableGHS05: CorrosiveGHS07: Exclamation mark
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
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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Infobox references


Phenyllithium was first produced by the reaction of lithium metal with diphenylmercury:[4]

(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.


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:[5]

C6H5Li + C5H5N → C6H5-C5H4N + LiH

Structure and propertiesEdit

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.[6]


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. Ph


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.[7]


  1. ^ "phenyllithium (CHEBI:51470)". Chemical Entities of Biological Interest (ChEBI). Cambridge, UK: European Bioinformatics Institute. 2009-01-22. Main. Retrieved 2013-06-01.
  2. ^ Wietelmann, U.; Bauer, R. J. "Lithium and Lithium Compounds". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a15_393.
  3. ^ 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.
  4. ^ 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.
  5. ^ Evans, J. C. W.; Allen, C. F. H. "2-Phenylpyridine" Organic Syntheses (1938), vol. 18, p. 70 doi:10.15227/orgsyn.018.0070
  6. ^ 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.
  7. ^ 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.