Mixing
Ylide
A ylide or ylid (/ˈɪlɪd/) 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. The result can be viewed as a structure in which two adjacent atoms are connected by both a covalent and an ionic bond; normally written X+–Y−. Ylides are thus 1,2-dipolar compounds, and a subclass of zwitterions.[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 Non-symmetric phosphorus ylides
4 Other types
4.1 Based on sulfur
4.2 Based on oxygen
4.3 Based on nitrogen
4.4 Other
5 Reactions
5.1 Dipolar cycloadditions
5.2 Dehydrocoupling with silanes
5.3 Sigmatropic rearrangements
5.4 Allylic rearrangements
6 See also
7 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
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.
Phosphorus ylides are important reagents in organic chemistry, especially in the synthesis of naturally occurring products with
biological and pharmacological activities. Much of the interest in the coordination properties of a-keto stabilized phosphorus
ylides stems from their coordination versatility due to the presence of different functional groups in their molecular structure.
Non-symmetric phosphorus ylides
The a-keto stabilized ylides derived from bisphosphines like dppe, dppm, etc., viz., [Ph2PCH2PPh2]C(H)C(O)R and [Ph2PCH2CH2PPh2]C(H)C(O)R (R = Me, Ph or OMe) constitute an important class of hybrid ligands containing both phosphine and ylide functionalities, and can exist in ylidic and enolate forms. These ligands can therefore be engaged in different kinds of bonding with metal ions like palladium and platinum.[3]
Other types
Based on sulfur
Other common ylides 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 or by reaction of carbonyls with electrophilic carbenes,[4] which are usually prepared from diazo compounds. Oxonium ylides (RR'-O+-C−R'R) are formed by the reaction of ethers with electrophilic carbenes.
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.
A rather exotic family of dinitrogen-based ylides are the isodiazenes: R1R2N+=N–. The generally decompose by extrusion of dinitrogen.
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.
Reactions
An important ylide reaction is of course the Wittig reaction (for phosphorus) but there are more.
Dipolar cycloadditions
Some ylides 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.[5] This reaction produces H2 gas a by product, and forms a silyl-stabilised ylide.
Sigmatropic rearrangements
Many ylides react in sigmatropic reactions.[6] 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 ylides[7][8]
Allylic rearrangements
Wittig reagents are found to react as nucleophiles in SN2' substitution:[9]
The initial addition reaction is followed by an elimination reaction.
See also
- 1,3-dipole
Betaine: a neutral molecule with an onium cation and a negative charge
Zwitterion: a neutral molecule with one or more pairs of positive and negative charges
References
^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "ylides". doi:10.1351/goldbook.Y06728
^ McMurry, John (2008). Organic Chemistry, 7th Ed. Thomson Brooks/Cole. pp. 720–722. ISBN 978-0-495-11258-7..mw-parser-output cite.citation{font-style:inherit}.mw-parser-output .citation q{quotes:"""""""'""'"}.mw-parser-output .citation .cs1-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .citation .cs1-lock-limited a,.mw-parser-output .citation .cs1-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .citation .cs1-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration{color:#555}.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration span{border-bottom:1px dotted;cursor:help}.mw-parser-output .cs1-ws-icon a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/4/4c/Wikisource-logo.svg/12px-Wikisource-logo.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output code.cs1-code{color:inherit;background:inherit;border:inherit;padding:inherit}.mw-parser-output .cs1-hidden-error{display:none;font-size:100%}.mw-parser-output .cs1-visible-error{font-size:100%}.mw-parser-output .cs1-maint{display:none;color:#33aa33;margin-left:0.3em}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-format{font-size:95%}.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-right{padding-right:0.2em}
^ Sabouncheia, Seyyed Javad; Ahmadi, Mohsen; Nasri, Zahra; Shams, Esmaeil; Salehzadeh, Sadegh; Gholiee, Yasin; Karamian, Roya; Asadbegy, Mostafa; Samiee, Sepideh (2013). "Synthesis, characterization, thermal, electrochemical, and DFT studies of mononuclear cyclopalladated complexes containing bidentate phosphine ligands and their biological evaluation as antioxidant and antibacterial agents". Comptes Rendus Chimie. 16 (2): 159–175. doi:10.1016/j.crci.2012.10.006.
^ Padwa, Albert (2005). "Catalytic Decomposition of Diazo Compounds as a Method for Generating Carbonyl‐Ylide Dipoles". Helvetica Chimica Acta. 88 (6): 1357–1374. doi:10.1002/hlca.200590109.
^ Nako, Adi E.; White, Andrew J. P.; Crimmin, Mark R. (2013). "A metal–amide dependent, catalytic C–H functionalisation of triphenylphosphonium methylide". Chemical Science. 4: 691–695. doi:10.1039/C2SC21123H.
^ Sweeney, J. B. (2009). "Sigmatropic rearrangements of 'onium' ylides". Chemical Society Reviews. 38: 1027–1038. doi:10.1039/b604828p. PMID 19421580.
^ 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.
^ Patel, Ramesh M.; Argade, Narshinha P. (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.
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