Strecker Amino Acid Synthesis

时间: Invalid Date
作者: 百灵威
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Strecker Amino Acid Synthesis-百灵威

The Strecker amino acid synthesis generates an α-amino acid from hydrogen cyanide, water, an aldehyde or ketone, and a 1° amine or ammonia. The carbonyl compound is first converted to an iminium ion, which is attacked by the cyanide ion to form an α-amino nitrile intermediate. Hydrolysis of the nitrile yields the α-amino acid.

  • Reagents: Hydrogen or Alkali Cyanide (KCN, NaCN) in Buffered Aqueous Media, Water
  • Reactant: Aliphatic/Aryl Ketone or Aldehyde, 1° or 2° Amine or Ammonia
  • Product: α-Amino Acid
  • Type of Reaction: Condensation
Mechanism
Original Paper
Top Citations
Related Reactions
  • Bucherer-Bergs Reaction
  • Petasis-Reaction
  • Multicompornent Reactions
  • Synthesis of α-aminonitriles
Related Compounds
  • Metal Cyanide
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