L-Serine methyl ester hydrochloride

A. Schouten, M. Lutz

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Esterification of the carboxyl group of amino acids plays an important role in the synthesis of peptides, especially due to the increased solubility in non-aquous organic solvents (Bodanszky, 1993). The synthesis of methyl esters is straightforward and can be performed by the reaction of HCl gas with a suspension of the amino acid in methanol. In this reaction the hydrochloride of the amino acid methyl ester is obtained, which is the subject of the present study.
Original languageUndefined/Unknown
Pages (from-to)o3026 Sup 1-o3026 Sup 7
Number of pages9
JournalActa crystallographica. Section E, Structure reports
VolumeE65
Publication statusPublished - 2009

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