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A convenient synthesis of amino acid methyl esters.

Molecules (Basel, Switzerland) (2008-06-19)
Jiabo Li, Yaowu Sha
ZUSAMMENFASSUNG

A series of amino acid methyl ester hydrochlorides were prepared in good to excellent yields by the room temperature reaction of amino acids with methanol in the presence of trimethylchlorosilane. This method is not only compatible with natural amino acids, but also with other aromatic and aliphatic amino acids.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Chlorotrimethylsilan, ≥98.0% (GC)
Sigma-Aldrich
Chlorotrimethylsilan, purified by redistillation, ≥99%
Sigma-Aldrich
Chlorotrimethylsilan, produced by Wacker Chemie AG, Burghausen, Germany, ≥99.0% (GC)
Sigma-Aldrich
Chlorotrimethylsilan, puriss., ≥99.0% (GC)
Sigma-Aldrich
Methyl-4-(aminomethyl)benzoat -hydrochlorid, 97%
Sigma-Aldrich
Chlortrimethylsilan -Lösung, 1.0 M in THF