VITAMINS
Online ISSN : 2424-080X
Print ISSN : 0006-386X
BENZOYLATION OF THIAMINE-DISULFIDE
Chikataro KAWASAKIIsao TOMITAIsamu DAIRA
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1962 Volume 25 Issue 1 Pages 61-63

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Abstract
By benzoylation of thiamine-disulfide (I), at least two products were obtained : Tetrabenzoate of (I), mp. 97-100℃ by the excess amount of benzoyl chloride and dibenzoate of (I), mp. 146-147℃ by the limited use of benzoyl chloride both in a pyridine or alkaline solution of (I), were isolated. Tetrabenzoate is sparingly soluble in acidic water and its structure is designated as (II) from its analytical value and infrared-spectrum. Beside dibenzoate (benzoylthiamine-disulfide) (III), a crystalline mixture of an unsharp mp. of 117-138℃ was obtained, when the reaction was carried out under ice-cooling. It contains two products, as its paper partition chromatogram indicated two spots ; Rf 0.57 and 0.74,of which 0.74 coincides with benzoylthiamine-disulfide.
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© 1962 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
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