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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503541Generated: October 30, 2026

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

https://huagongshe.com/reaction/1503541

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 H2O 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 numberUS09212163B2
Source datasetuspto-grants-2015_12
ORD IDord-90068ccc37154d928ebff777b7ca2b01
Source noteuspto-grants-2015_12