HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396945Generated: October 29, 2026
Potassium Hydroxide → 2-Amino-5-fluorobenzene-1-thiol
https://huagongshe.com/reaction/396945
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Amino-6-fluorobenzothiazole | HCID 319954 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-5-fluorobenzene-1-thiol | HCID 320547 | 99.7% |
Reaction Steps
In a 2,000-ml flask as a reactor were placed 166.7 g of water, 589.3 g of a 50% aqueous potassium hydroxide solution (5.25 moles as KOH) and 168.2 g (1.00 mole) of 6-fluoro-2-aminobenzothiazole. They were heated, aged for 8 hours with refluxing at 113 to 115° and then cooled to 40° C. The resulting mixture was washed with 311 g of toluene and then subjected to phase separation to obtain 904.0 g of an aqueous solution of a potassium salt of 2-amino-5-fluorothiophenol (concentration: 20%, yield: 99.7%). This aqueous solution of a potassium salt of 2-amino-5-fluorothiophenol can be used for production of a p-toluenesulfonate of [2-(6-fluorobenzothiazolyl)]ethylamine or an aqueous solution of [2-(6-fluorobenzothiazolyl)]ethylamine hydrochloride, according to the description in Example 1 to Example 7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06608207B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-7c12c43c14d14233ae761aedcae91568 |
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| Source note | uspto-grants-2003_08 |
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