Process for preparing N-acetyl-L-tyrosine
A technology of acetyltyrosine and tyrosine, which is applied in the field of amino acid preparation, can solve the problems of large amount of solvent, low purity of crude products, environmental pollution and the like, and achieves the effects of easy disposal of three wastes, short technological process and high purity
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[0008] Since L-Tyr has α-NH 2 and aromatic nucleus -OH two acylating groups, the former is weaker in electronegativity than the latter, easier to acetylate, and the N-Ac bond formed is more stable than the O-Ac bond. During the acylation reaction, in order to acylate the aromatic nucleus -OH group as little as possible, the formed O-Ac bond can be hydrolyzed in the subsequent process. For this reason, we prefer to use a medium-strength acetylating agent-acetic anhydride as the acylating agent.
[0009] The L-tyrosine and acetic anhydride with a weight ratio of 1:3~5 are acylated in an aqueous medium, the reaction temperature is controlled between 50-80°C, and the reaction time is controlled between 45-75 minutes. After 60 minutes, recover the solvent, and dry it by centrifugation, that is, the reaction solution after the acylation, vacuum the acid, and control the vacuum degree and temperature. The vacuum degree is 80-100mmhg, and the temperature is 75-80°C. O-Ac generated d...
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