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HRID 1089882作成日:2026年10月27日

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

https://huagongshe.com/reaction/1089882

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US05079368
出典データセットuspto-grants-1992_01
ORD IDord-cc20e8dfc8854d2d8ee0d340034eb4b1
出典メモuspto-grants-1992_01