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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089882Generated: October 26, 2026

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

https://huagongshe.com/reaction/1089882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant5-amino-6-fluorobenzo[d]thiazol-2(3H)-oneHCID 14458685—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
Product6-Fluoro-2(3H)-benzothiazolon-5-ylhydrazineHCID 1477163847%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05079368
Source datasetuspto-grants-1992_01
ORD IDord-cc20e8dfc8854d2d8ee0d340034eb4b1
Source noteuspto-grants-1992_01