HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222308Generated: October 30, 2026
Potassium Carbonate → 4-[(Pyridin-2-yl)sulfanyl]aniline
https://huagongshe.com/reaction/2222308
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Fluoro-5-nitrobenzotrifluoride | HCID 94954 | — |
| Reactant | 3-Trifluoromethyl-4-(4-pyridinylthio)nitrobenzene | HCID 23023084 | — |
| Reactant | pyridine-4-thiol | HCID 178418431 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[(Pyridin-2-yl)sulfanyl]aniline | HCID 18971660 | 54% |
Reaction Steps
3-(Trifluoromethyl)-4-(4-pyridinylthio)nitrobenzene: A solution of 4-mercaptopyridine (2.8 g, 24 mmoles), 2-fluoro-5-nitrobenzotrifluoride (5 g, 23.5 mmoles), and potassium carbonate (6.1 g, 44.3 mmoles) in anhydrous DMF (80 mL) was stirred at room temperature and under argon overnight. TLC showed complete reaction. The mixture was diluted with Et2O (100 mL) and water (100 mL) and the aqueous layer was back-extracted with Et2O (2×100 mL). The organic layers were washed with a saturated NaCl solution (100 mL), dried (MgSO4), and concentrated under reduced pressure. The solid residue was triturated with Et2O to afford the desired product as a tan solid (3.8 g, 54%): TLC (30% EtOAc/70% hexane) Rf 0.06; 1H-NMR (DMSO-d6) δ 7.33 (dd, J=1.2, 4.2 Hz, 2H), 7.78 (d, J=8.7 Hz, 1H), 8.46 (dd, J=2.4, 8.7 Hz, 1H), 8.54-8.56 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07371763B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-9dacd276d3974ca79f026f796c28e7d9 |
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| Source note | uspto-grants-2008_05 |
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