Pummerer rearrangement

The Pummerer rearrangement is an organic reaction whereby an alkyl sulfoxide rearranges to an α-acyloxy–thioether (monothioacetal-ester) in the presence of acetic anhydride.[1][2][3]

The Pummerer rearrangement
The Pummerer rearrangement
Pummerer rearrangement
Named after Rudolph Pummerer
Reaction type Rearrangement reaction
Identifiers
RSC ontology ID RXNO:0000220

The stoichiometry of the reaction is:

RS(O)CHR'2 + Ac2O → RSC(OAc)R'2 + AcOH

Synthetic implementation

Aside from acetic anhydride, trifluoroacetic anhydride and trifluoromethanesulfonic anhydride have been employed as activators.[4] Common nucleophiles besides acetates are arenes, alkenes, amides, and phenols.

The usage of α-acyl sulfoxides and Lewis acids, such as TiCl4 and SnCl4, allow the reaction to proceed at lower temperatures (0 °C).[5]

Thionyl chloride can be used in place of acetic anhydride to trigger the elimination for forming the electrophilic intermediate and supplying chloride as the nucleophile to give an α-chloro-thioether:[6]

Example of the Pummerer rearrangement using thionyl chloride
Example of the Pummerer rearrangement using thionyl chloride

Other anhydrides and acyl halides can give similar products. Inorganic acids can also give this reaction. This product can be converted to aldehyde or ketone by hydrolysis.[7]

Mechanism

The mechanism of the Pummerer rearrangement begins with the acylation of the sulfoxide (resonance structures 1 and 2) by acetic anhydride to give 3, with acetate as byproduct. The acetate then acts as a catalyst to induce an elimination reaction to produce the cationic-thial structure 4, with acetic acid as byproduct. Finally, acetate attacks the thial to give the final product 5.

The mechanism of the Pummerer rearrangement
The mechanism of the Pummerer rearrangement

The activated thial electrophile can be trapped by various intramolecular and intermolecular nucleophiles to form carbon–carbon bonds and carbon–heteroatom bonds.

The intermediate is so electrophilic that even neutral nucleophiles can be used, including aromatic rings with electron donating groups such as 1,3-benzodioxole:[8]

Example of the Pummerer rearrangement using veratrole
Example of the Pummerer rearrangement using veratrole

It is possible to perform the rearrangement using selenium in the place of sulfur.[9]

Pummerer fragmentation

When a substituent on the α position can form a stable carbocation, this group rather than the α-hydrogen atom will eliminate in the intermediate step. This variation is called a Pummerer fragmentation.[10] This reaction type is demonstrated below with a set of sulfoxides and trifluoroacetic anhydride (TFAA):

Pummerer fragmentation
Pummerer fragmentation

The organic group "R2" shown in the diagram above on the bottom right is the methyl violet carbocation, whose pKR+ of 9.4 is not sufficient to out-compete loss of H+ and therefore a classical Pummerer rearrangement occurs. The reaction on the left is a fragmentation because the leaving group with pKR+ = 23.7 is particularly stable.

History

The reaction was discovered by Rudolf Pummerer, who reported it in 1909.[11][12]

See also

References
  1. de Lucchi, Ottorino; Miotti, Umberto; Modena, Giorgio (1991). The Pummerer Reaction of Sulfinyl Compounds. pp. 157–184. doi:10.1002/0471264180.or040.03. ISBN 978-0471264187. {{cite book}}: |journal= ignored (help)
  2. Padwa, Albert; Gunn, David E. Jr.; Osterhout, Martin H. (1997). "Application of the Pummerer Reaction Toward the Synthesis of Complex Carbocycles and Heterocycles". Synthesis. 1997 (12): 1353–1377. doi:10.1055/s-1997-1384.
  3. Padwa, Albert; Bur, Scott K.; Danca, Diana M.; Ginn, John D.; Lynch, Stephen M. (2002). "Linked Pummerer-Mannich Ion Cyclizations for Heterocyclic Chemistry". Synlett. 2002 (6): 851–862. doi:10.1055/s-2002-31891.
  4. Smith, Laura H. S.; Coote, Susannah C.; Sneddon, Helen F.; Procter, David J. (2010). "Beyond the Pummerer Reaction: Recent Developments in Thionium Ion Chemistry". Angewandte Chemie International Edition. 49 (34): 5832–44. doi:10.1002/anie.201000517. PMID 20583014.
  5. Stamos, Ioannis K. (1986). "Arylation of α-phosphoryl sulfides via their pummerer rearrangement intermediates generated from the corresponding sulfoxides". Tetrahedron Letters. 27 (51): 6261–6262. doi:10.1016/S0040-4039(00)85447-7.
  6. Kosugi, Hiroshi; Watanabe, Yasuyuki; Uda, Hisashi (1989). "Lewis Acid-Mediated Carbon-Carbon bond forming reaction using the Pummerer Rearrangement Products from Chiral beta-Hydroxy Sulfoxides". Chemistry Letters. 18 (10): 1865–1868. doi:10.1246/cl.1989.1865.
  7. Meffre, Patrick; Durand, Philippe; Le Goffic, François (1999). "Methyl (S)-2-phthalimido-4-methylthiobutanoate". Organic Syntheses. 76: 123. doi:10.15227/orgsyn.076.0123.
  8. Ishibashi, Hiroyuki; Miki, Yumiko; Ikeda, Yoshiaki; Kiriyama, Akiko; Ikeda, Masazumi (1989). "Synthesis of α-(Methylthio)arylacetamides and Their Conversion into Some Biologically Active Arylethylamines". Biological & Pharmaceutical Bulletin. 37 (12): 3396–3398. doi:10.1248/cpb.37.3396.
  9. Gilmour, Ryan; Prior, Timothy J.; Burton, Jonathan W.; Holmes, Andrew B. (2007). "An organocatalytic approach to the core of eunicellin". Chemical Communications (38): 3954–6. doi:10.1039/B709322E. PMID 17896044.
  10. Laleu, Benoît; Santarém Machado, Marco; Lacour, Jérôme (25 May 2006). "Pummerer fragmentation vs. Pummerer rearrangement: a mechanistic analysis". Chemical Communications (26): 2786–2788. doi:10.1039/b605187a. PMID 17009463.
  11. Pummerer, Rudolph (1909). "Über Phenyl-sulfoxyessigsäure". Chemische Berichte. 42 (2): 2282–2291. doi:10.1002/cber.190904202126.
  12. Pummerer, Rudolph (1910). "Über Phenylsulfoxy-essigsäure. (II.)". Chemische Berichte. 43 (2): 1401–1412. doi:10.1002/cber.19100430241.
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