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Arndt-Eister reaction

  • Page ID
    66870
  • The Arndt–Eistert synthesis is a series of chemical reactions designed to convert a carboxylic acid to a higher carboxylic acid homologue (i.e. contains one additional carbon atom) and is considered a homologation process. Named for the German chemists Fritz Arndt (1885–1969) and Bernd Eistert (1902–1978), Arndt–Eistert synthesis is a popular method of producing β-amino acids from α-amino acids. Acid chlorides react with diazomethane to give diazoketones. In the presence of a nucleophile (water) and a metal catalyst (Ag2O), diazoketones will form the desired acid homologue.

    Overview of the Arndt–Eistert reaction

    While the classic Arndt–Eistert synthesis uses thionyl chloride to convert the starting acid to an acid chloride, any procedure can be used that will generate an acid chloride.

    Diazoketones are typically generated as described here, but other methods such as diazo-group transfer can also apply.

    Since diazomethane is toxic and violently explosive, many safer alternatives have been developed, such as the usage of ynolates (Kowalski ester homologation) or diazo(trimethylsilyl)methane.

    Reaction mechanism

    The key step in the Arndt–Eistert synthesis is the metal-catalyzed Wolff rearrangement of the diazoketone to form a ketene. In the insertion homologation of t-BOC protected (S)-phenylalanine (2-amino-3-phenylpropanoic acid), t-BOC protected (S)-3-amino-4-phenylbutanoic acid is formed.

    Homologation of N-boc-phenylalanine

    Wolff rearrangement of the α-diazoketone intermediate forms a ketene via a 1,2-rearrangement, which is subsequently hydrolysed to form the carboxylic acid. The consequence of the 1,2-rearrangement is that the methylene group alpha to the carboxyl group in the product is the methylene group from the diazomethane reagant. It has been demonstrated that the rearrangement preserves the stereochemistry of the chiral centre as the product formed from t-BOC protected (S)-phenylalanine retains the (S) stereochemistry with a reported enantiomeric excess of at least 99%.

    Heat, light, platinum, silver, and copper salts will also catalyze the Wolff rearrangement to produce the desired acid homologue.

    Variations

    In the Newman–Beal modification, addition of triethylamine to the diazomethane solution will avoid the formation of α-chloromethylketone side-products.