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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496016Generated: October 29, 2026

Potassium Carbonate → 4-(pyridin-4-ylsulfanyl)aniline

https://huagongshe.com/reaction/496016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-AminothiophenolHCID 14510—
Reactant4-Chloropyridine hydrochlorideHCID 81852—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-(pyridin-4-ylsulfanyl)anilineHCID 1132162878%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-aminothiophenol (20.2 g, 156.5 mmol) in anhydrous DMF (200 mL) was added 4-chloropyridine hydrochloride (24.4 g, 161.0 mmol) followed by potassium carbonate (44 g, 318.4 mmol). The reaction mixture was heated at 80° C. overnight, then diluted with ethyl acetate (400 mL) and water (400 mL). The aqueous layer was back-extracted with ethyl acetate (2×200 mL). The combined organic layers were washed with a saturated aqueous NaCl solution (200 mL), dried over anhy MgSO4, and concentrated under reduced pressure. The residue was filtered through a pad of silica with ethyl acetate and the resulting material was triturated with an ethyl ether/hexane solution to afford the desired product (24.7 g, 78%). TLC (50% ethyl acetate/50% hexane) Rf 0.25; 1H-NMR (DMSO-d6) δ 5.67 (bs, 2H), 6.65 (d, J=8.4 Hz, 2H), 6.88 (d, J=6.2 Hz, 2H), 7.19 (d, J=8.4 Hz, 2H), 8.27 (d, J=6.2 Hz, 2H), MS[M+H]+=203.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06943172B2
Source datasetuspto-grants-2005_09
ORD IDord-411758b93db7465dbe17c3865e3036a6
Source noteuspto-grants-2005_09