有機合成化学協会誌
Online ISSN : 1883-6526
Print ISSN : 0037-9980
ISSN-L : 0037-9980
2,3,5,6-テトラクロルフェニル酢酸の生成および合成
西山 隆三
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ジャーナル フリー

1967 年 25 巻 8 号 p. 677-680

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2, 3, 5, 6-Tetrachloroaniline was diazotized in a mixture of acetic acid and sulfuricacid according to the conventional procedures. The diazonium solution was then added dropwise into 700% sulfuric acid at 150-160°C, and the products were steamdistilled as soon as they were formed. Upon purification of the solids in the distillate, a small amount of colorless crystals (mp 212-213°C) showing a marked biological activity was obtained. This substance proved to be a new compound, 2, 3, 5, 6-tetrachlorophenylacetic acid. In the light of the fact that diazonium compounds usually decompose into phenols via diazonium ions, it is of interest to note that 2, 3, 5, 6-tetrachlorophenylacetic acid was obtained instead of 2, 3, 5. 6-tetrachlorophenol.

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