Horner-Wadsworth-Emmons reaction

The Horner-Wadsworth-Emmons reaction (or HWE reaction) is the chemical reaction of stabilized phosphonate carbanions with aldehydes (or ketones) to produce predominantly E-alkenes.

In 1958, Leopold Horner published a modified Wittig reaction using phosphonate-stabilized carbanions. [Leopold Horner; Hoffmann, H. M. R.; Wippel, H. G. "Ber." 1958, "91", 61-63.] [Horner, L.; Hoffmann, H. M. R.; Wippel, H. G.; Klahre, G. "Ber." 1959, "92", 2499-2505.] William S. Wadsworth and William D. Emmons further defined the reaction. [Wadsworth, W. S., Jr.; Emmons, W. D. "J. Am. Chem. Soc." 1961, "83", 1733. (DOI|10.1021/ja01468a042)] [Wadsworth, W. S., Jr.; Emmons, W. D. "Organic Syntheses", Coll. Vol. 5, p.547 (1973); Vol. 45, p.44 (1965). ( [http://www.orgsyn.org/orgsyn/prep.asp?prep=cv5p0547 Article] )]

In contrast to phosphonium ylides used in the Wittig reaction, phosphonate-stabilized carbanions are more nucleophilic and more basic. Likewise, phosphonate-stabilized carbanions can be alkylated, unlike phosphonium ylides. The dialkylphosphate salt byproduct is easily removed by aqueous extraction.

Several reviews have been published. [Wadsworth, W. S., Jr. "Org. React." 1977, "25", 73-253. (Review)] [Boutagy, J.; Thomas, R. "Chem. Rev." 1974, "74", 87-99. (Review, DOI|10.1021/cr60287a005)] [Kelly, S. E. "Comp. Org. Syn." 1991, "1", 729-817. (Review)] [B. E. Maryanoff; Reitz, A. B. "Chem. Rev." 1989, "89", 863-927. (Review, DOI|10.1021/cr00094a007)]

Reaction mechanism

The Horner-Wadsworth-Emmons reaction begins with the deprotonation of the phosphonate to give the phosphonate carbanion 1. Nucleophilic addition of the carbanion onto the aldehyde 2 (or ketone) producing 3a or 3b is the rate-limiting step. [Larsen, R. O.; Aksnes, G. "Phosphorus Sulfur" 1983, "15", 218-219.] If R₂=H, then intermediates 3a and 4a and intermediates 3b and 4b can interconvert with each other. [Lefèbvre, G.; Seyden-Penne, J. "J. Chem Soc., Chem. Commun." 1970, 1308-1309.] The final elimination of 4a and 4b yield E-alkene 5 and Z-alkene 6.

The ratio of alkene isomers 5 and 6 is dependent upon the stereochemical outcome of the initial carbanion addition and upon the ability of the intermediates to equilibrate.

The electron-withdrawing group (EWG) alpha to the phosphonate is necessary for the final elimination to occur. In the absence of an electron-withdrawing group, the final product is the α-hydroxyphosphonate 3a and 3b. [Corey, E. J.; Kwiatkowski, G. T. "J. Am. Chem. Soc." 1966, "88", 5654-5656. (DOI|10.1021/ja00975a057)] However, these α-hydroxyphosphonates can be transformed to alkenes by reaction with diisopropylcarbodiimide. [Reichwein, J. F.; Pagenkopf, B. L. "J. Am. Chem. Soc." 2003, "125", 1821-1824. (DOI|10.1021/ja027658s)]

tereoselectivity

The Horner-Wadsworth-Emmons reaction favours the formation of E-alkenes. In general, the more equilibration amongst intermediates, the higher the selectivity for E-alkene formation.

Disubstituted alkenes

Thompson and Heathcock have performed a systematic study of the reaction of trimethyl phosphonoacetate with various aldehydes. [Thompson, S. K.; Heathcock, C. H. "J. Org. Chem." 1990, "55", 3386-3388. (DOI|10.1021/jo00297a076)] While each effect was small, they had a cumulative effect making it possible to modify the stereochemical outcome without modifying the structure of the phosphonate. They found greater E-stereoselectivity with the following conditions:
* Increasing steric bulk of the aldehyde
* Higher reaction temperatures (23 °C over -78 °C)
* Li > Na > K salts
* Using the solvent DME over THF

In a separate study, it was found that bulky phosphonate and bulky electron-withdrawing groups enhance E-alkene selectivity.

Trisubstituted alkenes

The steric bulk of the phosphonate and electron-withdrawing groups plays a critical role in the reaction of α-branched phosphonates with aliphatic aldehydes. [Nagaoka, H.; Kishi, Y. "Tetrahedron" 1981, "37", 3873-3888.]

Aromatic aldehydes produce almost exclusively E-alkenes. In case Z-alkenes from aromatic aldehydes are needed, the Still modification (see below) can be used.

Olefination of ketones

The stereoselectivity of the Horner-Wadsworth-Emmons reaction of ketones is poor to modest.

Variations

Base sensitive substrates

Since many substrates are not stable to sodium hydride, several procedures have been developed using milder bases. Masamune and Roush have developed mild conditions using lithium chloride and DBU. [Blanchette, M. A.; Choy, W.; Davis, J. T.; Essenfeld, A. P.; Masamune, S.; Roush, W. R.; Sakai, T. "Tetrahedron Lett." 1984, "25", 2183-2186.] Rathke extended this to lithium or magnesium halides with triethylamine. [Rathke, M. W.; Nowak, M. "J. Org. Chem." 1985, "50", 2624-2626. (DOI|10.1021/jo00215a004)] Several other bases have been found effective. [Paterson, I.; Yeung, K.-S.; Smaill, J. B. "Synlett" 1993, 774.] [Simoni, D.; Rossi, M.; Rondanin, R.; Mazzali, A.; Baruchello, R.; Malagutti, C.; Roberti, M.; Invidiata, F. P. "Org. Lett." 2000, "2", 3765-3768.] [Blasdel, L. K.; Myers, A. G. "Org. Lett." 2005, "7", 4281-4283.]

till modification

Still and Gennari have developed conditions that give Z-alkenes with excellent stereoselectivity. [Still, W. C.; Gennari, C. "Tetrahedron Lett." 1983, "24", 4405-4408.] Using phosphonates with electron-withdrawing groups (trifluoroethyl [Patois, C.; Savignac, P.; About-Jaudet, E.; Collignon, N. "Organic Syntheses", Coll. Vol. 9, p.88 (1998); Vol. 73, p.152 (1996). ( [http://www.orgsyn.org/orgsyn/prep.asp?prep=cv9p0088 Article] )] ) together with strongly dissociating conditions (KHMDS and 18-crown-6 in THF) nearly exclusive Z-alkene production can be achieved.

Ando has suggested that the use of electron-deficient phosphonates accelerates the elimination of the oxaphosphatane intermediates. [Ando, K. "J. Org. Chem." 1997, "62", 1934–1939. (DOI|10.1021/jo970057c)]

References

ee also

*Michaelis-Arbusov reaction
*Michaelis-Becker reaction
*Peterson reaction
*Tebbe olefination