Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 2-Chloro-3-nitro-5-(trifluoromethyl)pyridine | HCID 4736950 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178526654 | HCID 178526654 | 79.5% |
Reaction Steps
A mixture of 4.88 g of 2-chloro3-nitro-5-(trifluoromethyl)pyridine, 1.81 g of thiourea and 40 ml of ethanol was stirred at 50° C. for 5.5 hours. The reaction mixture was cooled down to room temperature, then, concentrated under reduced pressure. To the residue was added 24 ml of water and a mixture of 2.8 g of sodium hydroxide and 6 ml of water, and this was stirred at room temperature for 1.5 hours. The reaction mixture was washed with diethyl ether, then, acetic acid was added. This was cooled with ice, and the deposited solid was collected by filtration. This solid was dried under reduced pressure, to obtain 3.84 g of 3-nitro-5-(trifluoromethyl)pyridine-2-thiol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08742112B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-f690258d91474877a5abf82723a8015d |
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| Source note | uspto-grants-2014_06 |
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