Organocopper compound

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Lithium diphenylcuprate etherate dimer from crystal structure
Skeletal formula of lithium diphenylcuprate etherate dimer

Organocopper compounds in organometallic chemistry contain carbon to copper chemical bonds. Organocopper chemistry is the science of organocopper compounds describing their physical properties, synthesis and reactions.[1][2][3] 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 copper(I) chloride solution:[4]

C2H2 + 2 CuCl → Cu2C2 + 2 HCl

Structure and bonding[edit]

Organocopper compounds are diverse in structure and reactivity, but organocopper compounds are largely limited in oxidation states to copper(I), sometimes denoted Cu+1. 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[edit]

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.[5]

Part of the framework of CuCl(CO). In this coordination polymer, the Cu centers are tetrahedral linked by triply bridging chloride ligands.

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.[6]

Although copper does not form a metallocene, half-sandwich complexes can be produced. One such derivative is (η-cyclopentadienyl triethylphosphine) copper.[7] This compound is a relatively rare example of an organocopper complex that follows the 18-electron rule.

Alkyl and aryl copper compounds[edit]

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 [CuRn](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 these difficulties, organocopper reagents are frequently generated and consumed in situ with no attempt to isolate them. They are used very frequently in organic chemistry 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.

Structures of simple alkyl and aryl copper compounds[edit]

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 mesitylpentacopper, 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.[8]

Organocopper aggregates

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, [{Li(OEt2)}(CuPh2)]2, in the solid state.[9]

Reactions of organocuprates[edit]

Cross-coupling reactions[edit]

Prior to the development of palladium-catalyzed cross coupling reaction, copper was the preferred catalyst for almost a century. Palladium offers faster more selective reaction. Although in the recent years copper compounds have appeared again as a synthetically useful as well as an eco-friendly metal, its low cost.[10]

Reactions of R2CuLi with alkyl halides R'-X gives the coupling product:

R2CuLi + R'X → R-R' + CuR + LiX

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

Many electrophiles participate in this reaction. The approximate order of reactivity, beginning with the most reactive, is as follows: acid chlorides[11] aldehydes > tosylates ~ epoxides > iodides > bromides > chlorides > ketones > esters > nitriles >> alkenes

Generally the OA-RE mechanism is analogous to palladium-catalyzed cross coupling reactions. One difference between copper and palladium is that copper can undergo single electron transfer processes.[12]

Copper cross coupling proposed mechanism

Coupling reactions[edit]

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'.[13][14]

Decarboxylative aryl-aryl coupling

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.

Conjugate addition[edit]

In 1941, Kharash discovered that Grignard reagents add to cyclohexenone in presence of Cu(I) resulting in 1,4-addition instead of 1,2-addition.[15] This work foreshadowed extensive studies on the conjugate additions to enones with organocuprates. Note that if a Grignard reagent (such as RMgBr) is used, the reaction with an enone would instead proceed through a 1,2-addition.[16] The 1,4-addition mechanism of cuprates to enones goes through the nucleophilic addition of the Cu(I) species at the beta-carbon of the alkene to form a Cu(III) intermediate, followed by reductive elimination of Cu(I).[17] In the original paper describing this reaction, methylmagnesium bromide is reacted with isophorone with and without 1 mole percent of added copper(I) chloride (see figure).[15]

Addition of methylmagnesium bromide to isophorone.[15]

Without added salt the main products are alcohol B (42%) from nucleophilic addition to the carbonyl group and diene C (48%) as its dehydration reaction product. With added salt the main product is 1,4-adduct A (82%) with some C (7%).

A 1,6-addition is also possible, for example in one step of the commercial-scale production of fulvestrant:[18]

Fulvestrant organic synthesis brazier 2010

Cu(III) intermediates[edit]

The involvement of the otherwise rare Cu(III) oxidation state has been demonstrated in the conjugate addition of the Gilman reagent to an enone:[19] 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 [20] 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.

A Cu(III) intermediate characterized by NMR.[19]


Carbocupration is a nucleophilic addition of organocopper reagents (R-Cu) to acetylene or terminal alkynes resulting in an alkenylcopper compound (RC=C-Cu).[21] It is a special case of carbometalation and also called the Normant reaction.[22]

Figure: Catalytic cycle for carbocupration Muller,.[23]

Carbocupration mechanism

Synthetic applications[edit]

Coupling involving aryl halides[edit]

"Ullmann chemistry" is involves formation of carbon-carbon bonds from aryl halides in the presence of a copper compound.[24]

Two types of Ullmann reaction are recognized:

  • Classic copper-promoted synthesis of symmetric biaryl compounds)
  • Copper-promoted nucleophilic aromatic substitution. Electronegative groups in the ortho position of the aryl halogen are strongly activated toward these reactions.[25] On the other hand, this reaction is inhibited by the steric hindrance provided by bulky groups on ortho positions of the aryl groups.

Ullman cond

Ullman synthesis of biaryl compounds can be employed to asymmetric reaction conditions.[26] Nelson and collaborators worked on the synthesis of asymmetric biaryl compounds and obtained the thermodynamically controlled product.[26]

Ullman Asymmetric reaction

The diastereometric rate of the product is enhanced with bulkier R groups in the auxiliary oxazoline group. Tert-butyl group has higher level of selectivity in the Ullman Coupling. Using an oxazoline auxiliary group provides steric effect which influences the high diastereoselectivity of asymmetric Ullman reaction.

Biphenyls had been obtained before with reasonable yields using 2, 2 diiodobiphenyl or 2, 2 diiodobiphenylonium ion as starting material; the reaction proceed when heating with Cu0 or Cu2O.

Ullman Byphenyl Synthesis

Closure of 5-membered ring are more favorable more facile, but larger rings have also been made using this approach.

Ring close sonogashira

Thermal dimerization proceeds via a copper hydride mechanism with complete retention of organocopper configuration.[12] Copper hydride proposed mechanism

Oxidative dimerization proceeds via oxidation of dialkylcuprate I to neutral transient diakyl copper (II) which decomposes to give the desired akyl alkyl dimer. This reaction is first order kinetics for both the organocopper and the substrate with inversion as the stereochemical consequence.SN2 like mechanism for oxidative dimerization and direct displacement

Oxid dimer

Direct displacement[edit]

Reactions with alkyl halides and organocopper compound are examples of direct displacement mechanism. As in an SN2 reaction, inversion of configuration occurs, as in oxidative dimerization. On the other hand, reactions of organocopper compound with alkenyl halides proceed with retention of subtrate’s configuration. Two possible mechanisms have been considered.[12] In the case of organocopper coupling with aryl halides the reaction proceed via aromatic nucleophilic substitution reaction. These reactions are reported to occur with lithium diaryl cuprates with a transmetalation step that forms mixed homocuprate compounds. The composition of this mixture can be generally determined statistically from the amount of substrate that is present before oxidation.

  • Organocopper and aryl halides coupling general mechanism

Sonogashira cross coupling reaction[edit]

The Sonogashira coupling reaction utilizes both copper and palladium. Its main synthetic application is the coupling of aryl and/or vinyl halides with terminal alkynes. The resulting alkynes are used for a variety of applications including click chemistry. Illustrating the Sonogashira cross coupling reactions is in the synthesis of imidazopyridine derivatives.[27] Imidazopyridine

A general mechanism for the Pd-Cu transmetallation in the Sonogashira cross coupling reaction is shown below.[28]

Pc-cu sonogash

Chan-Lam coupling reaction[edit]

The Chan-Lam reaction enables the formation of aryl carbon-hetoroatom bonds. It involves oxidative coupling of boronic acids, stannanes, or siloxanes with NH- or OH-containing substrates.[29]

Reducing agents[edit]

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)CuH]6. It reduces the alkene α,β-unsaturated carbonyl compounds.[30]

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.[23][31]

Buchwald selective- copper based chemistry

Synthesis of Z-Fluoro alkene dipeptide isosteres,.[32][33] Other effort to make this a more selective reactions includes the use of oxidation reduction condition for the reaction.[34] Fluoride acts as a leaving group and it enhances regioselectivity in the transformation the Z- fluoroalkene.

Z flouroalkene

Cu alkylation reaction[edit]

γ- Alkylation of allylic alcohols.[35]

Generally, the alkylation reaction of organocopper reagents proceed via gamma- alkylation. Cis- gamma attack occurs better in cyclohexyl carbamate due to sterics.

Alkylation of allylic alcohols

Alkylation of amines using the Gilman reagent Yamamoto and coworkers described an efficient synthetic method for the alkylation of amines. The reaction is based on the oxidative coupling of lithium alkyl copper amide which is reported to form in situ during the reaction between lithium dialkylcuprates and primary or secondary amides.[36]

Amine alkylation reaction

Cooper based Amine alkylation

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.[36]

Vicinal functionalization reactions[edit]

Vicinal functionalization using a Carbocupration- Mukaiyama aldol reaction sequence [37]

Vicinal funct

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.

See also[edit]

  • Chemistries of carbon with other elements of the periodic table:
Fr CRa Rf Db CSg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
Ac CTh CPa CU CNp CPu CAm CCm CBk CCf CEs Fm Md No Lr
Chemical bonds to carbon
Core organic chemistry Many uses in chemistry
Academic research, but no widespread use Bond unknown


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