HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587260Generated: October 26, 2026
Pyridine → 2-(4-Vinylphenoxy)isoindoline-1,3-dione
https://huagongshe.com/reaction/587260
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | 4-Vinylphenylboronic acid | HCID 2734393 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-Vinylphenoxy)isoindoline-1,3-dione | HCID 86675194 | 63% |
Reaction Steps
To a stirred solution of 4-vinylphenylboronic acid (2 g, 13 mmol), 2-hydroxyisoindoline-1,3-dione (3.63 g, 24.53 mmol), and CuCl (1.214 g 12.26 mmol) in 1,2-dichloroethane (50 mL) was added pyridine (1.065 g, 13.48 mmol), and the resultant reaction mixture was stirred at ambient temperature for 48 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. Purification by flash column chromatography (SiO2; 20% EtOAc in petroleum ether) afforded the title compound as a white solid (2 g, 63%): mp 129-131° C.; 1H NMR (400 MHz, CDCl3) δ 7.93 (d, J=2.0 Hz, 2H), 7.82 (d, J=3.2 Hz, 2H), 7.38 (d, J=2.0 Hz, 2H), 7.14 (d, J=2.0 Hz, 2H), 6.70 (m, 1H), 5.83 (d, J=16.0 Hz, 1H), 5.22 (d, J=10.8 Hz, 1H); ESIMS m/z 266.12 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09226500B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-ab7f74191dd74531978e73c74ecb66a8 |
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| Source note | uspto-grants-2016_01 |
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