HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503713Generated: October 28, 2026
p-Vinylbenzyl chloride → 2-[(4-Ethenylphenyl)methyl]-1H-isoindole-1,3(2H)-dione
https://huagongshe.com/reaction/1503713
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Vinylbenzyl chloride | HCID 74126 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[(4-Ethenylphenyl)methyl]-1H-isoindole-1,3(2H)-dione | HCID 19766639 | 46% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212164B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-da84ef4401a74fe9872686e47ef302c9 |
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| Source note | uspto-grants-2015_12 |
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