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Merck

A convenient synthesis of amino acid methyl esters.

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

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.

MATERIALES
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Sigma-Aldrich
Clorotrimetilsilano, ≥98.0% (GC)
Sigma-Aldrich
Clorotrimetilsilano, purified by redistillation, ≥99%
Sigma-Aldrich
Clorotrimetilsilano, produced by Wacker Chemie AG, Burghausen, Germany, ≥99.0% (GC)
Sigma-Aldrich
Clorotrimetilsilano, puriss., ≥99.0% (GC)
Sigma-Aldrich
Methyl 4-(aminomethyl)benzoate hydrochloride, 97%
Sigma-Aldrich
Chlorotrimethylsilane solution, 1.0 M in THF