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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502992Generated: October 30, 2026

p-Vinylbenzyl chloride → 2-[(4-Ethenylphenyl)methyl]-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/1502992

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Vinylbenzyl chlorideHCID 74126—
ReactantPhthalimide potassium saltHCID 24194345—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-[(4-Ethenylphenyl)methyl]-1H-isoindole-1,3(2H)-dioneHCID 1976663946%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a stirred solution of 1-(chloromethyl)-4-vinylbenzene (10 g, 66 mmol) in DMF (100 mL) was added potassium phthalimide (13.3 g, 72.1 mmol), and the resultant reaction mixture was heated at 70° C. for 16 h. The reaction mixture was diluted with water and extracted with CHCl3. The combined CHCl3 layer was washed with brine, dried over Na2SO4 and concentrated under reduced pressure. Recrystallization from CH3OH afforded the title compound as an off-white solid (8 g, 46%): 1H NMR (400 MHz, CDCl3) δ 7.83 (m, 2H), 7.71 (m, 2H), 7.39 (m, 4H), 6.65 (dd, J=17.6, 10.8 Hz, 1H), 5.72 (d, J=17.6 Hz, 1H), 5.21 (d, J=10.8 Hz, 1H), 4.82 (s, 2H); GCMS m/z 263.2 ([M]+); IR (thin film) 3420, 1133, 718 cm−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09211281B2
Source datasetuspto-grants-2015_12
ORD IDord-f547e34fb69a47b8b4f0d4aba2ff062d
Source noteuspto-grants-2015_12