Tebbe's reagent

Tebbe's reagent
Names
	IUPAC name μ-Chloro[di(cyclopenta-2,4-dien-1-yl)]dimethyl(μ-methylene)titaniumaluminum
	Other names Tebbe reagent
Identifiers
CAS Number	67719-69-1 ;
3D model (JSmol)	Interactive image;
ChemSpider	34981139 ;
ECHA InfoCard	100.157.162
PubChem CID	53384502;
UNII	V040SDB67S ;
CompTox Dashboard (EPA)	DTXSID50894875 ;
	InChI InChI=1S/2C5H5.2CH3.CH2.Al.Cl.Ti/c21-2-4-5-3-1;;;;;;/h21-5H;21H3;1H2;;;/q2-1;;;;-1;+1;+2 Key: FHPQZKBPAZOMGO-UHFFFAOYSA-N ; InChI=1/2C5H5.2CH3.CH2.Al.Cl.Ti/c21-2-4-5-3-1;;;;;;/h21-5H;21H3;1H2;;;/q2-1;;;;-1;+1;+2/r2C5H5.C3H8AlClTi/c21-2-4-5-3-1;1-4(2)3-6-5-4/h21-5H;3H2,1-2H3/q2*-1;+2 Key: FHPQZKBPAZOMGO-SBUAZLESAR;
	SMILES C[Al-]1(C[Ti+2][Cl+]1)C.[cH-]1cccc1.[cH-]1cccc1;
Properties
Chemical formula	C13H18AlClTi
Molar mass	284.60 g/mol
Solubility in other solvents	toluene, benzene, dichloromethane,; THF (low temperatures only)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Tebbe's reagent is the organometallic compound with the formula (C₅H₅)₂TiCH₂ClAl(CH₃)₂. It is used in the methylidenation of carbonyl compounds, that is it converts organic compounds containing the R₂C=O group into the related R₂C=CH₂ derivative.^[1] It is a red solid that is pyrophoric in the air, and thus is typically handled with air-free techniques. It was originally synthesized by Fred Tebbe at DuPont Central Research.

Tebbe's reagent contains two tetrahedral metal centers linked by a pair of bridging ligands. The titanium has two cyclopentadienyl ([C
₅H
₅]⁻
, or Cp) rings and aluminium has two methyl groups. The titanium and aluminium atoms are linked together by both a methylene bridge (-CH₂-) and a chloride atom in a nearly square-planar (Ti–CH₂–Al–Cl) geometry.^[2] The Tebbe reagent was the first reported compound where a methylene bridge connects a transition metal (Ti) and a main group metal (Al).^[3]

Preparation

The Tebbe reagent is synthesized from titanocene dichloride and trimethylaluminium in toluene solution.^[3]^[4]

Cp₂TiCl₂ + 2 Al(CH₃)₃ → CH₄ + Cp₂TiCH₂AlCl(CH₃)₂ + Al(CH₃)₂Cl

After about 3 days, the product is obtained after recrystallization to remove Al(CH₃)₂Cl.^[3] Although syntheses using the isolated Tebbe reagent give a cleaner product, successful procedures using the reagent "in situ" have been reported.^[5]^[6] Instead of isolating the Tebbe reagent, the solution is merely cooled in an ice bath or dry ice bath before adding the starting material.

An alternative but less convenient synthesis entails the use of dimethyltitanocene (Petasis reagent):^[7]

Cp₂Ti(CH₃)₂ + Al(CH₃)₂Cl → Cp₂TiCH₂AlCl(CH₃)₂ + CH₄

One drawback to this method, aside from requiring Cp₂Ti(CH₃)₂, is the difficulty of separating product from unreacted starting reagent.

Reaction mechanism

Tebbe's reagent itself does not react with carbonyl compounds, but must first be treated with a mild Lewis base, such as pyridine, which generates the active Schrock carbene.

Also analogous to the Wittig reagent, the reactivity appears to be driven by the high oxophilicity of Ti(IV). The Schrock carbene (1) reacts with carbonyl compounds (2) to give a postulated oxatitanacyclobutane intermediate (3). This cyclic intermediate has never been directly isolated, presumably because it breaks down immediately to the produce the desired alkene (5).

Scope

The Tebbe reagent is used in organic synthesis for carbonyl methylidenation.^[8] ^[9]^[10] This conversion can also be effected using the Wittig reaction, although the Tebbe reagent is more efficient especially for sterically encumbered carbonyls. Furthermore, the Tebbe reagent is less basic than the Wittig reagent and does not give the β-elimination products.

Methylidenation reactions also occur for aldehydes as well as esters, lactones and amides. The Tebbe reagent converts esters and lactones to enol ethers and amides to enamines. In compounds containing both ketone and ester groups, the ketone selectively reacts in the presence of one equivalent of the Tebbe reagent.

The Tebbe reagent methylidenates carbonyls without racemizing a chiral α carbon. For this reason, the Tebbe reagent has found applications in reactions of sugars where maintenance of stereochemistry can be critical.^[11]

The Tebbe reagent reacts with acid chlorides to form titanium enolates by replacing Cl⁻.

Modifications

It is possible to modify Tebbe's reagent through the use of different ligands. This can alter the reactivity of the complex, allowing for a broader range of reactions. For example, cyclopropanation can be achieved using a chlorinated analogue.^[12]

References

^ F. N. Tebbe, G. W. Parshall and G. S. Reddy (1978). "Olefin homologation with titanium methylene compounds". J. Am. Chem. Soc. 100 (11): 3611–3613. doi:10.1021/ja00479a061.
^ Thompson, Rick; Nakamaru-Ogiso, Eiko; Chen, Chun-Hsing; Pink, Maren; Mindiola, Daniel J. (2014). "Structural Elucidation of the Illustrious Tebbe Reagent". Organometallics. 33 (1): 429–432. doi:10.1021/om401108b.
^ ^a ^b ^c Herrmann, W.A., "The Methylene Bridge" Advances in Organometallic Chemistry 1982, 20, 195–197.
^ Straus, D. A., "μ-Chlorobis(cyclopentadienyl)(dimethylaluminium)-μ-methylenetitanium": Encyclopedia of Reagents for Organic Synthesis. John Wiley, London, 2000.
^ Pine, S. H.; Kim, V.; Lee, V. (1990). "Enol ethers by methylenation of esters: 1-Phenoxy-1-phenylethene and 3,4-dihydro-2-methylene-2H-1-benzopyran". Org. Synth. 69: 72. doi:10.15227/orgsyn.069.0072.
^ L. F. Cannizzo & R. H. Grubbs (1985). "In situ preparation of (μ-chloro)(μ-methylene)bis(cyclopentadienyl)(dimethylaluminum)titanium (Tebbe's reagent)". J. Org. Chem. 50 (13): 2386–2387. doi:10.1021/jo00213a040.
^ Payack, J. F.; Hughes, D. L.; Cai, D.; Cottrell, I. F.; Verhoeven, T. R. (2004). "Dimethyltitanocene". Organic Syntheses{{cite journal}}: CS1 maint: multiple names: authors list (link); Collected Volumes, vol. 10, p. 355.
^ Hartley, Richard C.; Li, Jianfeng; Main, Calver A.; McKiernan, Gordon J. (2007). "Titanium carbenoid reagents for converting carbonyl groups into alkenes". Tetrahedron. 63 (23): 4825–4864. doi:10.1016/j.tet.2007.03.015.
^ Pine, S. H. Org. React. 1993, 43, 1. (Review)
^ Beadham, I.; Micklefield, J. Curr. Org. Synth. 2005, 2, 231–250. (Review)
^ A. Marra, J. Esnault, A. Veyrieres and P. Sinay (1992). "Isopropenyl glycosides and congeners as novel classes of glycosyl donors: theme and variations". J. Am. Chem. Soc. 114 (16): 6354–6360. doi:10.1021/ja00042a010.{{cite journal}}: CS1 maint: multiple names: authors list (link)
^ Unusual Ambiphilic Carbenoid Equivalent in Amide Cyclopropanation Kuo-Wei Lin, Shiuan Yan, I-Lin Hsieh, and Tu-Hsin Yan Org. Lett.; 2006; 8(11) pp 2265 – 2267; Abstract
^ Luciano Lombardo (1987). "Methylenation of Carbonyl Compounds: (+)-3-Methylene-cis-p-menthane". Organic Syntheses. 65: 81. doi:10.15227/orgsyn.065.0081..