HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399850Generated: November 3, 2026
Hydrochloric Acid → 5-(trifluoromethyl)-1,3-benzothiazole-2-thiol
https://huagongshe.com/reaction/2399850
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | 2-Nitro-4-(trifluoromethyl)benzenethiol | HCID 117418 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(trifluoromethyl)-1,3-benzothiazole-2-thiol | HCID 178419087 | — |
Reaction Steps
Carbon disulphide (2.28 g, 30 mmol) was added dropwise over a period of 1 minute to a solution of potassium hydroxide (0.33 g, 5.9 mmol) in a mixture of water (2 ml) and methanol (5 ml), and the resulting yellow solution stirred for 5 minutes, followed by the addition of 2-nitro-4-trifluoromethyl thiophenol (1.10 g, 5 mmol). To this mixture was added dropwise over a period of 5 minutes a solution of potassium hydroxide (1.97 g, 35 mmol) and sodium dithionite (3.1 g, 15 mmol) in water (14 ml), so that the temperature did not exceed 40° C. The resultant orange mixture was stirred at 40°-50° C. for 2 hours. The reaction mixture was cooled to 10° C. and slowly acidified to pH 5-6 with concentrated HCl, and the mixture stirred for half an hour at this temperature. The off-white solid was washed with water and air dried to give the product. The yield was 0.81 g (70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05451681 |
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| Source dataset | uspto-grants-1995_09 |
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| ORD ID | ord-1b9be0a638d045c3886484a68c37371a |
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| Source note | uspto-grants-1995_09 |
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