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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477397Generated: October 25, 2026

Potassium Hydroxide → 6-fluoro-(3H)-benzo-thiazolon-5-ylhydrazine

https://huagongshe.com/reaction/477397

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-(3H)-benzo-thiazolon-5-ylhydrazineHCID 86743605—

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, fried over magnesium sulfate and concentrated by give 6-fluoro-(3H)-benzo-thiazolon-5-ylhydrazine (6 60 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04888045
Source datasetuspto-grants-1989_12
ORD IDord-b2fdeedc13884e18b546c7d5a2675ebc
Source noteuspto-grants-1989_12