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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587257Generated: October 30, 2026

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

https://huagongshe.com/reaction/587257

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 numberUS09226500B2
Source datasetuspto-grants-2016_01
ORD IDord-31aa7ef72bce42d094a463e86fd31293
Source noteuspto-grants-2016_01