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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-5-nitrobenzotrifluorideHCID 94954—
Reactant3-Trifluoromethyl-4-(4-pyridinylthio)nitrobenzeneHCID 23023084—
Reactantpyridine-4-thiolHCID 178418431—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product4-[(Pyridin-2-yl)sulfanyl]anilineHCID 1897166054%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371763B2
Source datasetuspto-grants-2008_05
ORD IDord-9dacd276d3974ca79f026f796c28e7d9
Source noteuspto-grants-2008_05