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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-amino-6-fluorobenzo[d]thiazol-2(3H)-one | HCID 14458685 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 6-fluoro-(3H)-benzo-thiazolon-5-ylhydrazine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04888045 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-b2fdeedc13884e18b546c7d5a2675ebc |
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| Source note | uspto-grants-1989_12 |
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