Arndt–Eistert reaction explained

In organic chemistry, the Arndt–Eistert reaction is the conversion of a carboxylic acid to its homologue. Named for the German chemists Fritz Arndt (1885 - 1969) and Bernd Eistert (1902 - 1978), the method entails treating an acid chlorides with diazomethane. It is a popular method of producing β-amino acids from α-amino acids.[1]

Conditions

Aside from the acid chloride substrate, three reagents are required: diazomethane, water, and a metal catalyst. Each has been well investigated.

The diazomethane is required in excess so as to react with the HCl formed previously. Not taking diazomethane in excess results in HCl reacting with the diazoketone to form chloromethyl ketone and N2. Mild conditions allow this reaction to take place while not affecting complex or reducible groups in the reactant-acid.[2]

The reaction requires the presence of a nucleophile (water). A metal catalyst is required. Usually Ag2O is chosen but other metals and even light effect the reaction.

Variants

The preparation of the beta-amino acid from phenylalanine illustrates the Arndt–Eistert synthesis carried out with the Newman–Beal modification, which involves the inclusion of triethylamine in the diazomethane solution. Either triethylamine or a second equivalent of diazomethane will scavenge HCl, avoiding the formation of α-chloromethylketone side-products.[3] [4]

Diazomethane is the traditional reagent, but analogues can also be applied.[5] Diazomethane is toxic and potentially violently explosive, which has led to safer alternative procedures,[6] For example, diazo(trimethylsilyl)methane has been demonstrated.[7] [8]

Acid anhydrides can be used in place of acid chloride. The reaction yields a 1:1 mixture of the homologated acid and the corresponding methyl ester.[9]

This method can also be used with primary diazoalkanes, to produce secondary α-diazo ketones. However, there are many limitations. Primary diazoalkanes undergo azo coupling to form azines; thus the reaction conditions must be altered such that acid chloride is added to a solution of diazoalkane and triethylamine at low temperature.[10] [11] In addition, primary diazoalkanes are very reactive, incompatible with acidic functionalities, and will react with activated alkenes including unsaturated carbonyls to give 1,3-dipolar cycloaddition products.

An alternative to the Arndt–Eistert reaction is the Kowalski ester homologation, which also involves the generation of a carbene equivalent but avoids diazomethane.[12]

Reaction mechanism

The acid chloride suffers attack by diazomethane with loss of HCl. The alpha-diazoketone (RC(O)CHN2) product undergoes the metal-catalyzed Wolff rearrangement to form a ketene, which hydrates to the acid.[13] [14] [15] The rearrangement leaves untouched the stereochemistry at the carbon alpha to the acid chloride.

Historical readings

See also

Notes and References

  1. Ye. T.. McKervey. M. A.. Organic Synthesis with α-Diazo Carbonyl Compounds. Chem. Rev.. 94. 4. 1091–1160. 1994. 10.1021/cr00028a010.
  2. Book: Reactions, Rearrangements and Reagents. Sanyal, S.N.. 4. 2003. 86, 87. 978-81-7709-605-7.
  3. Newman. M. S.. Melvin Spencer Newman. Beal. P. F.. J. Am. Chem. Soc.. An Improved Wolff Rearrangement in Homogeneous Medium. 72. 11. 5163–5165. 1950. 10.1021/ja01167a101.
  4. Clibbens, D. A. Nierenstein, M. . J. Chem. Soc.. 1915. 107. 1491–1494. 10.1039/ct9150701491. CLXV.—The action of diazomethane on some aromatic acyl chlorides.
  5. Rick L. Danheiser . Danheiser. R. L.. Miller. R. F.. Brisbois. R. G.. 10.15227/orgsyn.073.0134. Detrifluoroacetylative Diazo Group Transfer: (E)-1-Diazo-4-phenyl-3-buten-2-one. Organic Syntheses. 73. 134. 1996.
  6. Alan R. Katritzky. Katritzky. A. R.. Zhang. S.. Hussein. A. H. M.. Fang. Y.. Steel. P. J.. One-Carbon Homologation of Carboxylic Acids via BtCH2TMS: A Safe Alternative to the Arndt−Eistert Reaction. J. Org. Chem.. 2001. 66. 16. 5606–5612. 10.1021/jo0017640. 11485491.
  7. 10.1016/S0040-4039(00)92200-7. Aoyama. T.. Shiori. T.. New Methods and Reagents in Organic Synthesis. 8. Trimethylsilyldiazomethane. A New, Stable, and Safe Reagent for the Classical Arndt-Eistert Synthesis. Tetrahedron Lett.. 1980. 21. 46. 4461–4462.
  8. Cesar. J.. Dolenc. M. S.. Trimethylsilyldiazomethane in the Preparation of Diazoketones via Mixed Anhydride and Coupling Reagent Methods: A New Approach to the Arndt–Eistert Synthesis. Tetrahedron Lett.. 42. 40. 7099–7102. 2001. 10.1016/S0040-4039(01)01458-7.
  9. Bradley, W. Robinson, R. . J. Am. Chem. Soc.. 1930. 52. 1558–1565. 10.1021/ja01367a040. The Action of Diazomethane on Benzoic and Succinic Anhydrides, and a Reply to Malkin and Nierenstein. 4.
  10. Franzen, V. . Justus Liebigs Annalen der Chemie. 1957. 602. 199. 10.1002/jlac.19576020116. Eine neue Methode zur Darstellung α,β-ungesättiger Ketone. Zerfall der Diazoketone R—CO—CN2—CH2—R′.
  11. Yates, P. Farnum, D. G. Wiley, D. W. . Chem. Ind.. 1958. 69.
  12. Reddy. R. E.. Kowalski. C. J.. 71. 146. 1993. 10.15227/orgsyn.071.0146. Ethyl 1-Naphthylacetate: Ester Homologation Via Ynolate Anions. Organic Syntheses.
  13. The Mechanism of the Arndt-Eistert Reaction. C.. Huggett. R. T.. Arnold. T. I.. Taylor. J. Am. Chem. Soc.. 1942. 64. 12. 3043. 10.1021/ja01264a505.
  14. 1975. Angew. Chem. Int. Ed.. Meier. H.. Zeller. K.-P.. 14. 1. 32–43. 10.1002/anie.197500321. The Wolff Rearrangement of α-Diazo Carbonyl Compounds.
  15. 2002. Eur. J. Org. Chem.. Kirmse. W.. 2193–2256. 10.1002/1099-0690(200207)2002:14<2193::AID-EJOC2193>3.0.CO;2-D. 100 Years of the Wolff Rearrangement. 2002. 14.

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