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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1089882생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1089882

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물5-amino-6-fluorobenzo[d]thiazol-2(3H)-oneHCID 14458685—
반응물Sodium NitriteHCID 23668193—
용매Hydrochloric AcidHCID 313—
생성물6-Fluoro-2(3H)-benzothiazolon-5-ylhydrazineHCID 1477163847%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05079368
출처 데이터셋uspto-grants-1992_01
ORD IDord-cc20e8dfc8854d2d8ee0d340034eb4b1
출처 메모uspto-grants-1992_01