HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587741Generated: October 28, 2026
2,2'-Bipyridine → (E)-N-(2-chloro-4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-en-1-yl)benzyl)pyridin-2-amine
https://huagongshe.com/reaction/587741
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,2'-Bipyridine | HCID 1474 | — |
| Reactant | 1-(1-Bromo-2,2,2-trifluoroethyl)-3,4,5-trichlorobenzene | HCID 86675153 | — |
| Reactant | N-(2-chloro-4-vinylbenzyl)pyridin-2-amine | HCID 86675183 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | (E)-N-(2-chloro-4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-en-1-yl)benzyl)pyridin-2-amine | HCID 86675208 | 35% |
Reaction Steps
To a stirred solution of N-(2-chloro-4-vinylbenzyl)pyridin-2-amine (0.3 g, 1.22 mmol) in 1,2-dichlorobenzene (5 mL) were added 5-(1-bromo-2,2,2-trifluoroethyl)-1,2,3-trichlorobenzene (0.83 g, 2.44 mmol), CuCl (24 mg, 0.24 mmol) and 2,2-bipyridyl (76 mg, 0.48 mmol). The resultant reaction mixture was degassed with argon for 30 min and then stirred at 180° C. for 24 h. After the reaction was deemed complete by TLC, the reaction mixture was cooled to ambient temperature and filtered, and the filtrate was concentrated under reduced pressure. Purification by flash chromatography (SiO2, 100-200 mesh; 15% EtOAc in n-hexane) afforded the title compound as an off-white solid (0.2 g, 35%): mp 140-142° C.; 1H NMR (400 MHz, CDCl3) δ 8.11 (d, J=4.0 Hz, 1H), 7.40 (m, 5H), 7.22 (m, 1H), 6.61 (m, 2H), 6.35 (m, 2H), 4.94 (br s, 1H), 4.61 (d, J=6.4 Hz, 2H), 4.11 (m, 1H); ESIMS m/z 505.39 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09226501B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-0bae55b6e6014205b7bc559c9cf12ef3 |
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| Source note | uspto-grants-2016_01 |
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