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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502736Generated: October 29, 2026

Pyridine → 2-(4-Vinylphenoxy)isoindoline-1,3-dione

https://huagongshe.com/reaction/1502736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantN-HydroxyphthalimideHCID 10665—
Reactant4-Vinylphenylboronic acidHCID 2734393—
CatalystCuprous chlorideHCID 62652—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
Product2-(4-Vinylphenoxy)isoindoline-1,3-dioneHCID 8667519463%

Reaction Steps

To a stirred solution of 4-vinylphenylboronic acid (2 g, 13 mmol), 2-hydroxyisoindoline-1,3-dione (3.63 g, 24.53 mmol), and CuCl (1.214 g 12.26 mmol) in 1,2-dichloroethane (50 mL) was added pyridine (1.065 g, 13.48 mmol), and the resultant reaction mixture was stirred at ambient temperature for 48 h. The reaction mixture was diluted with H2O and extracted with CHCl3. The combined CHCl3 layer was washed with brine, dried over Na2SO4 and concentrated under reduced pressure. Purification by flash column chromatography (SiO2; 20% EtOAc in petroleum ether) afforded the title compound as a white solid (2 g, 63%): mp 129-131° C.; 1H NMR (400 MHz, CDCl3) δ 7.93 (d, J=2.0 Hz, 2H), 7.82 (d, J=3.2 Hz, 2H), 7.38 (d, J=2.0 Hz, 2H), 7.14 (d, J=2.0 Hz, 2H), 6.70 (m, 1H), 5.83 (d, J=16.0 Hz, 1H), 5.22 (d, J=10.8 Hz, 1H); ESIMS m/z 266.12 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09210927B2
Source datasetuspto-grants-2015_12
ORD IDord-4ff69f0b945f4807a819ae31a729cbba
Source noteuspto-grants-2015_12