Organocopper compound

Organocopper compounds is the chemistry of organometallic compounds containing a carbon to copper chemical bond. Organocopper chemistry is the study of organocopper compounds describing their physical properties, synthesis and reactions. They are reagents in organic chemistry.

The first organocopper compound, the explosive copper(I) acetylide Cu₂C₂ (Cu−C≡C−Cu), was synthesized by Rudolf Christian Böttger in 1859 by passing acetylene gas through a solution of copper(I) chloride:
:C₂H₂ + 2 CuCl → Cu₂C₂ + 2 HCl

Structure and bonding

Organocopper compounds are diverse in structure and reactivity, but organocopper compounds are largely limited in oxidation states to copper(I), sometimes denoted Cu⁺. As a d¹⁰ metal center, it is related to Ni(0), but owing to its higher oxidation state, it engages in less pi-backbonding. Organic derivatives of Cu(II) and Cu(III) are invoked as intermediates but rarely isolated or even observed. In terms of geometry, copper(I) adopts symmetrical structures, in keeping with its spherical electronic shell. Typically one of three coordination geometries is adopted: linear 2-coordinate, trigonal 3-coordinate, and tetrahedral 4-coordinate. Organocopper compounds form complexes with a variety of soft ligands such as alkylphosphines (R₃P), thioethers (R₂S), and cyanide (CN⁻).

Simple complexes with CO, alkene, and Cp ligands

Copper(I) salts have long been known to bind CO, albeit weakly. A representative complex is CuCl(CO), which is polymeric. In contrast to classical metal carbonyls, pi-backbonding is not strong in these compounds.

Alkenes bind to copper(I), although again generally weakly. The binding of ethylene to Cu in proteins is of broad significance in plant biology so much so that ethylene is classified as a plant hormone. Its presence, detected by the Cu-protein, affects ripening and many other developments.

Although copper does not form a metallocene, half-sandwich complexes can be produced. One such derivative is π-cyclopentadienyl(triethylphosphine)copper(I).

Alkyl and aryl copper compounds

Alkyl and aryl copper(I) compounds

Copper halides react with organolithium reagents to give organocopper compounds. The area was pioneered by Henry Gilman, who reported methylcopper in 1936. Thus, phenylcopper is prepared by reaction of phenyllithium with copper(I) bromide in diethyl ether. Grignard reagents can be used in place of organolithium compounds. Gilman also investigated the dialkylcuprates. These are obtained by combining two equivalent of RLi with Cu(I) salts. Alternatively, these cuprates are prepared from oligomeric neutral organocopper compounds by treatment with one equivalent of organolithium reagent.

Compounds of the type uR''_n''sup>(''n''-1)- are reactive towards oxygen and water, forming copper(I) oxide. They also tend to be thermally unstable, which can be useful in certain coupling reactions. Despite or because of these difficulties, organocopper reagents are frequently generated and consumed in situ with no attempt to isolate them. They are used in organic synthesis as alkylating reagents because they exhibit greater functional group tolerance than corresponding Grignard and organolithium reagents. The electronegativity of copper is much higher than its next-door neighbor in the group 12 elements, zinc, suggesting diminished nucleophilicity for its carbon ligands.

Copper salts react with terminal alkynes to form the acetylides.

Alkyl halides react with organocopper compounds with inversion of configuration. On the other hand, reactions of organocopper compound with alkenyl halides proceed with retention of subtrate’s configuration.

Organocopper compounds couple with aryl halides:
: $\begin \ce\ &\ce\\ \ce\ &\ce\\ \ce\ &\ce \end$

Structures

Alkyl and aryl copper complexes aggregate both in crystalline form and in solution. Aggregation is especially evident for charge-neutral organocopper compounds, i.e. species with the empirical formula (RCu), which adopt cyclic structures. Since each copper center requires at least two ligands, the organic group is a bridging ligand. This effect is illustrated by the structure of mesitylcopper, which is a pentamer. A cyclic structure is also seen for CuCH₂SiMe₃, first 1:1 organocopper compound to be analyzed by X-ray crystallography (1972 by Lappert). This compound is relatively stable because the bulky trimethylsilyl groups provide steric protection. It is a tetramer, forming an 8-membered ring with alternating Cu-C bonds. In addition the four copper atoms form a planar Cu₄ ring based on three-center two-electron bonds. The copper to copper bond length is 242 pm compared to 256 pm in bulk copper. In ''pentamesitylpentacopper'' a 5-membered copper ring is formed, similar to (2,4,6-trimethylphenyl)gold, and ''pentafluorophenylcopper'' is a tetramer.
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Lithium dimethylcuprate is a dimer in diethyl ether, forming an 8-membered ring with two lithium atoms linking two methyl groups. Similarly, lithium diphenylcuprate forms a dimeric etherate, CuPh₂)sub>2, in the solid state.

Alkyl and aryl copper(III) compounds

The involvement of the otherwise rare Cu(III) oxidation state has been demonstrated in the conjugate addition of the Gilman reagent to an enone: In a so-called rapid-injection NMR experiment at -100 °C, the Gilman reagent Me₂CuLi (stabilized by lithium iodide) was introduced to cyclohexenone (1) enabling the detection of the copper — alkene pi complex 2. On subsequent addition of trimethylsilyl cyanide the Cu(III) species 3 is formed (indefinitely stable at that temperature) and on increasing the temperature to -80 °C the conjugate addition product 4. According to an accompanying in silico experiments the Cu(III) intermediate has a square planar molecular geometry with the cyano group in cis orientation with respect to the cyclohexenyl methine group and anti-parallel to the methine proton. With other ligands than the cyano group this study predicts room temperature stable Cu(III) compounds.
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Reactions of organocuprates

Cross-coupling reactions

Prior to the development of palladium-catalyzed cross coupling reactions, copper was the preferred catalyst for almost a century. Palladium offers a faster, more selective reaction. However, in recent years copper has reemerged as a synthetically useful metal, because of its lower cost and because it is an eco-friendly metal.

Reactions of R₂CuLi with alkyl halides R'-X give the coupling product:
:R₂CuLi + R'X → R-R' + CuR + LiX

The reaction mechanism involves oxidative addition (OA) of the alkyl halide to Cu(I), forming a planar Cu(III) intermediate, followed by reductive elimination (RE). The nucleophilic attack is the rate-determining step. In the substitution of iodide, a single-electron transfer mechanism is proposed (see figure).

: ce\ce-\ce\ \xrightarrow\ \left ce R\overset\underset\ce \right-\ce \ce + \ce + \ce

Many electrophiles participate in this reaction. The approximate order of reactivity, beginning with the most reactive, is as follows: acid chlorides > aldehydes > tosylates ~ epoxides > iodides > bromides > chlorides > ketones > esters > nitriles >> alkenes

Generally the OA-RE mechanism is analogous to that of palladium-catalyzed cross coupling reactions. One difference between copper and palladium is that copper can undergo single-electron transfer processes.Posner, G. H. 2011. Substitution Reactions Using Organocopper Reagents. Organic Reactions. 22:2:253–400

Coupling reactions

Oxidative coupling is the coupling of copper acetylides to conjugated alkynes in the Glaser coupling (for example in the synthesis of cyclooctadecanonaene) or to aryl halides in the Castro-Stephens Coupling.

Reductive coupling is a coupling reaction of aryl halides with a stoichiometric equivalent of copper metal that occurs in the Ullmann reaction. In an example of a present-day cross coupling reaction called decarboxylative coupling, a catalytic amount of Cu(I) displaces a carboxyl group forming the arylcopper (ArCu) intermediate. Simultaneously, a palladium catalyst converts an aryl bromide to the organopalladium intermediate (Ar'PdBr), and on transmetallation the biaryl is formed from ArPdAr'.

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Redox neutral coupling is the coupling of terminal alkynes with halo-alkynes with a copper(I) salt in the Cadiot-Chodkiewicz coupling. Thermal coupling of two organocopper compounds is also possible.

Carbocupration

Carbocupration is a nucleophilic addition of organocopper reagents (R-Cu) to acetylene or terminal alkynes resulting in an alkenylcopper compound (RC=C−Cu). It is a special case of carbometalation and also called the Normant reaction.

Synthetic applications

*The Chan-Lam coupling enables the formation of aryl carbon-hetoroatom bonds. It involves coupling of boronic acids, stannanes, or siloxanes with NH- or OH-containing substrates.
*Ullmann reaction involves copper-mediated reactions of aryl halides. Two types of Ullmann reaction are recognized:
*#Classic copper-promoted synthesis of symmetric biaryl compounds)
*#Copper-promoted nucleophilic aromatic substitution.
*Sonogashira coupling reaction, which utilizes both copper and palladium, entails the coupling of aryl and/or vinyl halides with terminal alkynes.

Reducing agents

Copper hydrides are specialized reagents used occasionally as reducing agent. The best known copper hydride is called Stryker's reagent, a cluster compound with the formula PPh₃)CuHsub>6. It reduces the alkene α,β-unsaturated carbonyl compounds.

The Buchwald reaction is a copper-catalyzed asymmetric reduction of activated alkenes. The reagent is generated in situ from copper(I) NHC complex. The hydride equivalents are provided by a silane.
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Synthesis of Z-Fluoro alkene dipeptide isosteres,. Other effort to make this a more selective reactions includes the use of oxidation reduction condition for the reaction. Fluoride acts as a leaving group and it enhances regioselectivity in the transformation the Z- fluoroalkene.

Cu alkylation reaction

Generally, the alkylation reaction of organocopper reagents proceed via gamma- alkylation. Cis- gamma attack occurs better in cyclohexyl carbamate due to sterics. The reaction is reported to be favorable in ethereal solvents. This method was proved to be very effective for the oxidative coupling of amines and alkyl, including tertbutyl, and aryl halides.

Vicinal functionalization reactions

Vicinal functionalization using a Carbocupration- Mukaiyama aldol reaction sequence: Muller, A.J.; Jennings, M.P. Vicinal Functionalization of propionilate Esters via Tandem Catalytic Carbocupration-Mukaiyama Aldol Reaction sequence. Org. Lett. 2008, 10, 1649-1652

Muller and collaborators reported a vicinal functionalization of α,β- acetylenic esters using a carbocupration/Mukaiyama aldol reaction sequence (as shown in fig. above) carbocupration favors the formation of the Z- aldol.

Further reading

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References

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