ビタミン
Online ISSN : 2424-080X
Print ISSN : 0006-386X
Dibenzoylthiamineのメタノリシス : (I)DibenzoylthiamineよりO-Benzoylthiamineおよび安息香酸メチルの生成
川崎 近太郎堀尾 嘉友遠藤 登義
著者情報
ジャーナル フリー

1963 年 28 巻 2 号 p. 152-155

詳細
抄録
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℃.
著者関連情報
© 1963 日本ビタミン学会

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
前の記事 次の記事
feedback
Top