Ylide

An ylide or ylid (pronounced /ˈɪlɪd/ or /ˈɪlaɪd/) is a neutral dipolar molecule containing a formally negatively charged atom (usually a carbanion) directly attached to a hetero atom 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". The name "ylide" derives from the negatively charged carbon or alkyl moiety in the molecule which is given the "ide" suffix that denotes a negatively charged unit (c.f. chloride, oxide, nitride).

Contents

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

Phosphonium ylides are used in the Wittig reaction for double bond synthesis from carbonyl groups (C=O). The positive charge in these Wittig reagents is carried by a phosphorus atom with three phenyl substituents and one bond to a carbon bearing a negative charge and two substituents, commonly alkyl groups. Ylids can be 'stabilised' or 'non-stabilised'. Non-stabilised ylids react readily with both aldehydes and ketones whereas stabilised will only react with aldehydes . Stabilised ylids react with both aldehydes and ketones very rapidly in the HWE reaction.

A phosphonium ylide can be prepared rather straightforwardly. Typically, a phosphine (e.g. triphenylphosphine) is allowed to react with an alkyl halide in a mechanism analogous to that of an SN2 reaction. This forms an alkyltriphenylphosphonium salt which is then allowed to react with a strong base (in this case, dimsyl sodium) to form the ylide.

The salt products are not shown. Also, the product shown here is shown in the ylide form; however, it could also be shown as the phosphorane form in which the bond to phosphorus is a double bond with the methylene group. Due to an inductive effect, the trio of phenyl groups allows phosphorus to bear such a buildup of positive charge and shifts the negative charge to carbon, creating a reactive species.

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 sulfur

Other common ylids include sulfonium ylids and sulfoxonium ylids, 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 ylids (RR'-O+-C-R'R) are prepared by reaction of ethers with diazo compounds.

Based on nitrogen

Certain nitrogen-based ylids also exist such as azomethine ylids 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 ylids 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.

Sigmatropic rearrangements

Many ylids react in sigmatropic reactions.[3] 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 [4][5]

Allylic rearrangements

Wittig reagents are found to react as nucleophiles in SN2' substitution:[6]

The initial addition reaction is followed by an elimination reaction.

See also

References

  1. ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (2006–) "ylides".
  2. ^ McMurry, John (2008). Organic Chemistry, 7th Ed.. Thomson Brooks/Cole. pp. 720–722. ISBN 978-0-495-11258-7. 
  3. ^ Sigmatropic rearrangements of ‘onium’ ylids J. B. Sweeney Chem. Soc. Rev., 2009, 38, 1027–1038 doi:10.1039/b604828p
  4. ^ 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. 
  5. ^ (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 ylid. (iii) A rearrangement reaction (in blue) yields a phosphonate.
  6. ^ 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.