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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110073Generated: October 31, 2026

p-Fluoronitrobenzene → 4-[(Pyridin-2-yl)sulfanyl]aniline

https://huagongshe.com/reaction/2110073

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
Reactant4-phenyl-1,3-thiazole-2-thiolHCID 178527830—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-[(Pyridin-2-yl)sulfanyl]anilineHCID 18971660145.7%

Reaction Conditions

Temperature65 °C

Reaction Steps

4-(2-(4-Phenyl)thiazolyl)thio-1-nitrobenzene: A solution of 2-mercapto-4-phenylthiazole (4.0 g, 20.7 mmoles) in DMF (40 mL) was treated with 1-fluoro-4-nitrobenzene (2.3 mL, 21.7 mmoles) followed by K2CO3 (3.18 g, 23 mmol), and the mixture was heated at approximately 65° C. overnight. The reaction mixture was then diluted with EtOAc (100 mL), sequentially washed with water (100 mL) and a saturated NaCl solution (100 mL), dried (MgSO4) and concentrated under reduced pressure. The solid residue was triturated with a Et2O/hexane solution to afford the desired product (6.1 g): TLC (25% EtOAc/75% hexane) Rf 0.49; 1H-NMR (CDCl3) δ 7.35-7.47 (m, 3H), 7.58-7.63 (m, 3H), 7.90 (d, J=6.9 Hz, 2H), 8.19 (d, J=9.0 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517880B2
Source datasetuspto-grants-2009_04
ORD IDord-dc248d9bc82f4e608ff6f6403e657b72
Source noteuspto-grants-2009_04