VITAMINS
Online ISSN : 2424-080X
Print ISSN : 0006-386X
METHANOLYSIS OF DIBENZOYLTHIAMINE : (I) FORMATION OF METHYL BENZOATE AND O-BENZOYLTHIAMINE FROM DIBENZOYLTHIAMINE
Chikataro KAWASAKITakatomo HORIONoriyoshi ENDO
Author information
JOURNAL FREE ACCESS

1963 Volume 28 Issue 2 Pages 152-155

Details
Abstract
Dibenzoylthiamine (DBT) in methanol, when it is dissolved in 10mg% or 100mg% concentration and boiled for hours, is slowly decomposed into methyl benzoate (I), O-benzoyl-thiamine (II) and free thiamine to an extent of nearly 50% the complete methanolysis after 2 hour's boiling : (I) and (II) were detected in the solution by means of paper partition chromatography. (I) was distilled in vacuum from the reaction mixture and it was identified as benzoic acid after its saponification. Methanolysis of DBT is specific because other solvents such as ethanol, propanol, isobutanol and propylene glycol are incapable of similar alcoholysis of DBT. Ethylene glycol, however, can similarly decompose DBT, when the solution is kept at 65℃.
Content from these authors
© 1963 THE VITAMIN SOCIETY OF JAPAN

この記事はクリエイティブ・コモンズ [表示 - 非営利 - 改変禁止 4.0 国際]ライセンスの下に提供されています。
https://creativecommons.org/licenses/by-nc-nd/4.0/deed.ja
Previous article Next article
feedback
Top