Barbier reaction

The Barbier reaction is an organometallic reaction between an alkyl halide (chloride, bromide, iodide), a carbonyl group and a metal. The reaction can be performed using magnesium, aluminium, zinc, indium, tin, samarium, barium or their salts. The reaction product is a primary, secondary or tertiary alcohol. The reaction is similar to the Grignard reaction but the crucial difference is that the organometallic species in the Barbier reaction is generated in situ, whereas a Grignard reagent is prepared separately before addition of the carbonyl compound.[1] Unlike many Grignard reagents, the organometallic species generated in a Barbier reaction are unstable, necessitating their immediate usage. Barbier reactions are nucleophilic addition reactions that involve relatively inexpensive, water insensitive metals or metal compounds. For this reason it is possible in many cases to run the reaction in water, making the procedure part of green chemistry. In contrast, Grignard reagents and organolithium reagents are highly moisture sensitive and must be used under an inert atmosphere without the presence of water. The Barbier reaction is named after Victor Grignard's teacher Philippe Barbier.

Not to be confused with Barbier–Wieland degradation.
Barbier reaction
Named after Philippe Barbier
Reaction type Coupling reaction
Identifiers
RSC ontology ID RXNO:0000084
Barbier reaction with samarium(II) iodide

Scope

Examples of Barbier reactions are the reaction of propargylic bromide with butanal with zinc metal (the reaction is carried out in THF, the saturated aqueous ammonium chloride solution added later to quench the reaction):[2]

Barbier reaction
With a substituted alkyne instead of a terminal alkyne the allene product is favoured

the intramolecular Barbier reaction with samarium(II) iodide:[3]

Barbier reaction

the reaction of an allyl bromide with formaldehyde in THF with indium powder:[4]

Barbier reaction
The Barbier reaction is accompanied by an allylic rearrangement to a terminal alkene

The reaction of 3-Bromocyclohexene with benzaldehyde and zinc powder in water:[5]

Barbier reaction
The observed diastereoselectivity for this reaction is erythro : threo = 83 : 17

Asymmetric Variants
Main article: Asymmetric addition of dialkylzinc compounds to aldehydes

The synthesis of (+)-aspicillin, starts first with a hydroboration, then transmetallation to zinc which can then do an addition into the aldehyde substituent.[6]

The total synthesis of (+)-aspicillin involves a Barbier reaction

See also
  • Barbier reaction @ University of Connecticut Website

References
  1. Barbier, P. (1899). "Synthèse du diéthylhepténol". Compt. Rend. 128: 110.
  2. Artur Jõgi & Uno Mäeorg (2001). "Zn Mediated Regioselective Barbier Reaction of Propargylic Bromides in THF/aq. NH4Cl Solution". Molecules. 6 (12): 964–968. doi:10.3390/61200964.
  3. Tore Skjæret & Tore Benneche (2001). "Preparation of oxo-substituted α-chloro ethers and their reaction with samarium diiodide". Arkivoc: KU–242A.
  4. George D. Bennett and Leo A. Paquette. "Methyl 3-(hydroxymethyl)-4-methyl-2-methylenepentanoate". Organic Syntheses.; Collective Volume, 10, p. 77
  5. Gary W. Breton; John H. Shugart; Christine A. Hughey; Brian P. Conrad; Suzanne M. Perala (2001). "Use of Cyclic Allylic Bromides in the Zinc–Mediated Aqueous Barbier–Grignard Reaction". Molecules. 6 (8): 655–662. doi:10.3390/60800655.
  6. Oppolzer, Wolfgang; Radinov, Rumen N.; Brabander, Jef De (1995). "Total synthesis of the macrolide (+)-aspicilin by an asymmetrically catalyzed macrocyclization of an ω-Alkynal ester". Tetrahedron Letters. 36 (15): 2607–2610. doi:10.1016/0040-4039(95)00351-C.
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