Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587247Generated: October 29, 2026

Toluene → 2-((3-Chloro-5-vinylpyridin-2-yl)methyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/587247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium CarbonateHCID 11430—
Reactant2-((5-Bromo-3-chloropyridin-2-yl)methyl)isoindoline-1,3-dioneHCID 71138575—
CatalystHCID 178418397HCID 178418397—
Product2-((3-Chloro-5-vinylpyridin-2-yl)methyl)isoindoline-1,3-dioneHCID 8667518465%

Reaction Steps

To a stirred solution of 2-((5-bromo-3-chloropyridin-2-yl)methyl)isoindoline-1,3-dione (0.23 g, 0.65 mmol) in toluene (10 mL) were added Pd(PPh3)4 (3.7 mg, 0.003 mmol), K2CO3 (0.269 g, 1.95 mmol) and vinyl boronic anhydride pyridine complex (0.78 g, 3.28 mmol), and the reaction mixture was heated at reflux for 16 h. The reaction mixture was filtered, and the filtrate was washed with water and brine, dried over anhydrous Na2SO4, and concentrated under reduced pressure. Purification by flash column chromatography (20-30% EtOAc in hexane) afforded the title compound as an off-white solid (0.2 g, 65%): 1H NMR (400 MHz, CDCl3) δ 8.30 (s, 1H), 7.91 (m, 2H), 7.77 (m, 3H), 7.72 (m, 1H), 6.63 (m, 1H), 5.79 (d, J=16.0 Hz, 1H), 5.39 (d, J=16.0 Hz, 1H), 5.12 (s, 2H); ESIMS m/z 299.20 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226500B2
Source datasetuspto-grants-2016_01
ORD IDord-6e143a3690e440dfbc987da40e9b61b4
Source noteuspto-grants-2016_01