Strecker amino acid synthesis

Strecker synthesis
Named after Adolph Strecker
Reaction type Substitution reaction
Identifiers
Organic Chemistry Portal strecker-synthesis
RSC ontology ID RXNO:0000207

The Strecker amino acid synthesis, also known simply as the Strecker synthesis, is a method for the synthesis of amino acids by the reaction of an aldehyde with cyanide in the presence of ammonia. The condensation reaction yields an α-aminonitrile, which is subsequently hydrolyzed to give the desired amino acid. The method is used for the commercial production of racemic methionine from methional.

Primary and secondary amines also give N-substituted amino acids. Likewise, the usage of ketones, instead of aldehydes, gives α,α-disubstituted amino acids.