| 词条 | Barbier reaction |
| 释义 |
| Name = Barbier reaction | Type = Coupling reaction | NamedAfter = Philippe Barbier | Section3 = {{Reactionbox Identifiers | RSC_ontology_id = 0000084 }} 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. ScopeExamples 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] the intramolecular Barbier reaction with samarium(II) iodide:[3] the reaction of an allyl bromide with formaldehyde in THF with indium powder:[4] or another allyl bromide in a reaction with benzaldehyde and zinc powder in water:[5] Asymmetric Variants{{Main|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] See also
External links
References1. ^{{cite journal | author = Barbier, P. | url = http://gallica.bnf.fr/ark:/12148/bpt6k30841.pleinepage.f110.langFR | title = Synthèse du diéthylhepténol | journal = Compt. Rend. | year = 1899 | volume = 128 | pages = 110}} 2. ^{{cite journal | title = Zn Mediated Regioselective Barbier Reaction of Propargylic Bromides in THF/aq. NH4Cl Solution |author1=Artur Jõgi |author2=Uno Mäeorg |lastauthoramp=yes | journal = Molecules | year = 2001 | volume = 6 | pages = 964–968 | url = http://www.mdpi.org/molecules/papers/61200964.pdf | doi = 10.3390/61200964 | issue = 12 |issn=1420-3049}} 3. ^{{cite journal | title = Preparation of oxo-substituted α-chloro ethers and their reaction with samarium diiodide |author1=Tore Skjæret |author2=Tore Benneche |lastauthoramp=yes | journal = Arkivoc | pages = KU–242A | year = 2001 | url = http://www.arkat-usa.org/ark/journal/2001/I10_Undheim/242/242.asp }} 4. ^{{OrgSynth | title = Methyl 3-(hydroxymethyl)-4-methyl-2-methylenepentanoate | author = George D. Bennett and Leo A. Paquette | collvol = 10 | collvolpages = 77 | prep = v77p0107}} 5. ^{{cite journal | title = Use of Cyclic Allylic Bromides in the Zinc–Mediated Aqueous Barbier–Grignard Reaction |author1=Gary W. Breton |author2=John H. Shugart |author3=Christine A. Hughey |author4=Brian P. Conrad |author5=Suzanne M. Perala | journal = Molecules | year = 2001 | volume = 6 | pages = 655–662 | url = http://www.mdpi.org/molecules/papers/60800655.pdf | doi = 10.3390/60800655 | issue = 8}} 6. ^De Brabander,J;et al. Tetrahedron Letters, 1995, Vol. 36, No. 15, pp. 2607-2610 4 : Addition reactions|Free radical reactions|Carbon-carbon bond forming reactions|Name reactions |
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