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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587728Generated: October 28, 2026

1,2-Dimethoxyethane → 2-(4-Vinylphenylamino)isoindoline-1,3-dione

https://huagongshe.com/reaction/587728

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(4-bromoanilino)-1H-isoindole-1,3(2H)-dioneHCID 16044339—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product2-(4-Vinylphenylamino)isoindoline-1,3-dioneHCID 8667519113%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a solution of 2-(4-bromophenylamino)isoindoline-1,3-dione (2 g, 6 mmol) in 1,2-dimethoxyethane (20 mL) and water (4 mL) were added vinyl boronic anhydride pyridine complex (4.57 g, 18.98 mmol) and K2CO3 (1.3 g, 9.5 mmol) followed by Pd(PPh3)4 (0.219 g, 0.189 mmol). The resultant reaction mixture was heated at 150° C. in a microwave for 30 min and then was concentrated under reduced pressure. Purification by column chromatography (SiO2, 15% EtOAc in petroleum ether) afforded the title compound as a solid (200 mg, 13%): mp 174-176° C.; 1H NMR (400 MHz, CDCl3) δ 8.65 (s, 1H), 7.94 (m, 4H), 7.29 (d, J=8.4 Hz, 2H), 6.72 (d, J=8.4 Hz, 2H), 6.61 (m, 1H), 5.61 (d, J=17.6 Hz, 1H), 5.05 (d, J=11.2 Hz, 1H); ESIMS m/z 263.18 ([M−H]−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226501B2
Source datasetuspto-grants-2016_01
ORD IDord-af67348ea1ce4053bff6cbfa0edbeebb
Source noteuspto-grants-2016_01