An ylide or ylid (// or //) is a neutral dipolar molecule containing a formally negatively charged atom (usually a carbanion) directly attached to a heteroatom with a formal positive charge (usually nitrogen, phosphorus or sulfur), and in which both atoms have full octets of electrons. Ylides are thus 1,2-dipolar compounds.[1] They appear in organic chemistry as reagents or reactive intermediates.[2]
The class name "ylide" for the compound should not be confused with the suffix "-ylide".
Contents
- 1 Resonance structures
- 2 Phosphonium ylides
- 3 Other ylide types
- 3.1 Based on sulphur
- 3.2 Based on oxygen
- 3.3 Based on nitrogen
- 3.4 Other
- 4 Ylide reactions
- 4.1 Dipolar cycloadditions
- 4.2 Dehydrocoupling with silanes
- 4.3 Sigmatropic rearrangements
- 4.4 Allylic rearrangements
- 5 See also
- 6 References
Resonance structures
Many ylides may be depicted by a multiple bond form in a resonance structure, known as the ylene form:
The actual electron distribution in the molecules and hence the relative importance of the ylide and ylene forms is dependent on the "onium" center and substituent pattern (the identity of the various R groups).
Phosphonium ylides
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Structure of methylenetriphenylphosphorane.
Phosphonium ylides are used in the Wittig reaction, a method used to convert ketones and especially aldehydes to alkenes. The positive charge in these Wittig reagents is carried by a phosphorus atom with three phenyl substituents and a bond to a carbanion. Ylides can be 'stabilised' or 'non-stabilised'. A phosphonium ylide can be prepared rather straightforwardly. Typically, triphenylphosphine is allowed to react with an alkyl halide in a mechanism analogous to that of an SN2 reaction. This quaternization forms an alkyltriphenylphosphonium salt, which can be isolated or treated in situ with a strong base (in this case, butyl lithium) to form the ylide.
Due to the SN2 mechanism, a less sterically hindered alkyl halide reacts more favorably with triphenylphosphine than an alkyl halide with significant steric hindrance (such as tert-butyl bromide). Because of this, there will typically be one synthetic route in a synthesis involving such compounds that is more favorable than another.
Other ylide types
Based on sulphur
Other common ylids include sulfonium ylides and sulfoxonium ylides, for instance the Corey-Chaykovsky reagent used in the preparation of epoxides or in the Stevens rearrangement.
Based on oxygen
Carbonyl ylides (RR'C=O+C-RR') can form by ring-opening of epoxides. Oxonium ylides (RR'-O+-C-R'R) are prepared by reaction of ethers with diazo compounds.
Based on nitrogen
Certain nitrogen-based ylides also exist such as azomethine ylides with the general structure:
These compounds can be envisioned as iminium cations placed next to a carbanion. The substituents R1, R2 are electron withdrawing groups. These ylides can be generated by condensation of an α-amino acid and an aldehyde or by thermal ring opening reaction of certain N-substituted aziridines.
Stable carbenes also have a ylidic resonance contributor e.g.:
Other
Halonium ylides can be prepared from allyl halides and metal carbenoids. After a [2,3]-rearrangement a homoallylhalide is obtained.
The active form of Tebbe's reagent is often considered a titanium ylide. Like the Wittig reagent, it is able to replace the oxygen atom on carbonyl groups with a methylene group. Compared with the Wittig reagent, it has more functional group tolerance.
Ylide reactions
An important ylide reaction is of course the Wittig reaction (for phosphorus) but there are more.
Dipolar cycloadditions
Some ylids are 1,3-dipoles and interact in 1,3-dipolar cycloadditions. For instance an azomethine ylide is a dipole in the Prato reaction with fullerenes.
Dehydrocoupling with silanes
In the presence of the group 3 homoleptic catalyst Y[N{SiMe3)2}3], triphenylphosphonium methylide can be coupled with phenylsilane.[3] This reaction produces H2 gas a by product, and forms a silyl-stabilised ylide.
Sigmatropic rearrangements
Many ylids react in sigmatropic reactions.[4] The Sommelet-Hauser rearrangement is an example of a [2,3]-sigmatropic reaction. The Stevens rearrangement is a [1,2]-rearrangement.
A [3,3]-sigmatropic reaction has been observed in certain phosphonium ylids [5][6]
Allylic rearrangements
Wittig reagents are found to react as nucleophiles in SN2' substitution:[7]
The initial addition reaction is followed by an elimination reaction.
See also
- 1,3-dipole
- Zwitterion: a neutral molecule with one or more pairs of positive and negative charges
- Betaine: a neutral molecule with an onium cation and a negative charge
References
- ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "ylides".
- ^ McMurry, John (2008). Organic Chemistry, 7th Ed. Thomson Brooks/Cole. pp. 720–722. ISBN 978-0-495-11258-7.
- ^ A. E. Nako, A. J. P. White, M. R. Crimmin, Chem. Sci., 2013,4, 691-695, DOI: 10.1039/C2SC21123H
- ^ Sigmatropic rearrangements of ‘onium’ ylids J. B. Sweeney Chem. Soc. Rev., 2009, 38, 1027–1038 doi:10.1039/b604828p
- ^ Ferguson, Marcelle L.; Senecal, Todd D.; Groendyke, Todd M.; Mapp, Anna K. (2006). "[3,3]-Rearrangements of Phosphonium Ylides". J. Am. Chem. Soc. 128 (14): 4576–4577. doi:10.1021/ja058746q. PMID 16594686.
- ^ (i) Reaction of allyl alcohol with 2-chloro-5,5-dimethyl-1,3,2-dioxaphosphorinane forms a phosphite ester. (ii) Metal carbene addition (from ethyl diazoacetate and ClFeTPP) forms an ylide. (iii) A rearrangement reaction (in blue) yields a phosphonate.
- ^ Ramesh M. Patel and Narshinha P. Argade (2007). "Facile SN2' Coupling Reactions of Wittig Reagents with Dimethyl Bromomethylfumarate: Synthesis of Enes, Dienes, and Related Natural Products". J. Org. Chem. 72 (13): 4900–4904. doi:10.1021/jo070728z. PMID 17539690.
