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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503027Generated: October 31, 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/1503027

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2'-BipyridineHCID 1474—
Reactant1-(1-Bromo-2,2,2-trifluoroethyl)-3,4,5-trichlorobenzeneHCID 86675153—
ReactantN-(2-chloro-4-vinylbenzyl)pyridin-2-amineHCID 86675183—
CatalystCuprous chlorideHCID 62652—
Solvent1,2-DichlorobenzeneHCID 7239—
Product(E)-N-(2-chloro-4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-en-1-yl)benzyl)pyridin-2-amineHCID 8667520835%

Reaction Conditions

Temperature180 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09211281B2
Source datasetuspto-grants-2015_12
ORD IDord-6ea1b2d218864e909131e87a33f31c4a
Source noteuspto-grants-2015_12