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HRID 1995387作成日:2026年10月25日

Potassium Cyanide → 4-hydroxy-1H-1,2-benzisothiazole-1,1,3(2H)-trione

https://huagongshe.com/reaction/1995387

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CyanideHCID 9032—
反応物Sodium HydroxideHCID 14798—
反応物PotassiumHCID 5462222—
反応物4-Methoxy-1H-1lambda~6~,2-benzothiazole-1,1,3(2H)-trioneHCID 14984051—
反応物3-Amino-4-methoxy-1,2-benzoisothiazole-1,1-dioxideHCID 15567164—
溶媒Dimethyl SulfoxideHCID 679—
生成物4-hydroxy-1H-1,2-benzisothiazole-1,1,3(2H)-trioneHCID 148652262%

反応手順

2.5 gm (11.8 mmols) of 3-amino-4-methoxy-1,2-benzoisothiazole-1,1-dioxide were reacted with sodium hydroxide analogous to Example 5, and by subsequent acidification the reaction product was converted into 4-methoxy-1,2-benzoisothiazol-3(2H)-one-1,1-dioxide. The obtained compound, together with 650 mg (10 mmols) of potassium cyanide in dimethyl-sulfoxide, was heated at 180° C. for 3 hours. After addition of petroleum ether the potassium salt of the product was precipitated, and the precipitate was dissolved in water. After acidifying with aqueous hydrochloric acid, filtering and recrystallizing, 1.46 gm (62% of theory) of 4-hydroxy-1,2-benzoisothiazol-3(2H)-one-1,1-dioxide were obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04404230
出典データセットuspto-grants-1983_09
ORD IDord-9028caa34a404d9e8ab189188776807c
出典メモuspto-grants-1983_09