戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1709030作成日:2026年10月25日

Potassium Hydroxide → 6-Fluoro-2(3H)-benzothiazolon-5-ylhydrazine

https://huagongshe.com/reaction/1709030

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物5-amino-6-fluorobenzo[d]thiazol-2(3H)-oneHCID 14458685—
反応物Sodium NitriteHCID 23668193—
溶媒Hydrochloric AcidHCID 313—
生成物6-Fluoro-2(3H)-benzothiazolon-5-ylhydrazineHCID 1477163847%

反応手順

A suspension of 5-amino-6-fluoro-2(3H)-benzothiazolone (12.98 g) in conc. hydrochloric acid (70 g) was cooled to 0° to 5° C., and a saturated aqueous solution of sodium nitrite (5.08 g) was dropwise added thereto at 0° to 5° C., followed by stirring at the same temperature for 30 minutes. The resultant mixture was cooled to -20° C., and a solution of stannous chloride (28.06 g) in conc. hydrochloric acid (30 g) was added thereto all at once, followed by stirring at 0° C. for 2 hours. The reaction mixture was neutralized with potassium hydroxide, a colloidal substance originated from stannous chloride was removed by celite and the resultant solution was extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and concentrated to give 6-fluoro-2(3H)-benzothiazolon-5-ylhydrazine (6.60 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04946961
出典データセットuspto-grants-1990_08
ORD IDord-72adc180d26f4e7e89bcc32513f87f8e
出典メモuspto-grants-1990_08