Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587254Generated: October 29, 2026

2,2'-Bipyridine → (E)-2-((4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-en-1-yl)naphthalen-1-yl)methyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/587254

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2'-BipyridineHCID 1474—
Reactant1-(1-Bromo-2,2,2-trifluoroethyl)-3,4,5-trichlorobenzeneHCID 86675153—
Reactant2-((4-Vinylnaphthalen-1-yl)methyl)isoindoline-1,3-dioneHCID 86675188—
CatalystCuprous chlorideHCID 62652—
Solvent1,2-DichlorobenzeneHCID 7239—
Product(E)-2-((4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-en-1-yl)naphthalen-1-yl)methyl)isoindoline-1,3-dioneHCID 8667519056%

Reaction Conditions

Temperature180 °C

Reaction Steps

To a stirred solution of 2-((4-vinylnaphthalen-1-yl)methyl)isoindoline-1,3-dione (1.5 g, 4.79 mmol) in 1,2-dichlorobenzene (15 mL) were added 1-(1-bromo-2,2,2-trifluoroethyl)-3,4,5-trichlorobenzene (3.2 g, 9.5 mmol), CuCl (24 mg, 0.24 mmol) and 2,2-bipyridyl (0.149 g, 0.95 mmol), and the resultant reaction mixture was degassed with argon for 30 min and then stirred at 180° C. for 14 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; 25-30% EtOAc in petroleum ether) afforded the title compound as an off-white solid (1.5 g, 56%): mp 158-160° C.; 1H NMR (400 MHz, CDCl3) δ 8.40 (m, 1H), 7.89 (m, 2H), 7.74 (m, 2H), 7.64 (m, 2H), 7.58 (m, 2H), 7.46 (s, 2H), 7.36 (m, 2H), 6.31 (m, 1H), 5.30 (s, 2H), 4.21 (m, 1H); ESIMS m/z 572.08 ([M−H]−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226500B2
Source datasetuspto-grants-2016_01
ORD IDord-d312311861fa49338b7e8a012c45bdc8
Source noteuspto-grants-2016_01