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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-phenyl-1,3-thiazole-2-thiol | HCID 178527830 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-[(Pyridin-2-yl)sulfanyl]aniline | HCID 18971660 | 145.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07517880B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-dc248d9bc82f4e608ff6f6403e657b72 |
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| Source note | uspto-grants-2009_04 |
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