HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503545Generated: October 29, 2026
Potassium Carbonate → 2-(2-Chloro-4-vinylbenzyl)isoindoline-1,3-dione
https://huagongshe.com/reaction/1503545
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-4-((1,3-dioxoisoindolin-2-yl)methyl)benzaldehyde | HCID 86675178 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(2-Chloro-4-vinylbenzyl)isoindoline-1,3-dione | HCID 86675179 | 79.5% |
Reaction Steps
To a stirred solution of 3-chloro-4-((1,3-dioxoisoindolin-2-yl)methyl)benzaldehyde (2.8 g, 8.2 mmol) in 1,4-dioxane (30 mL) were added K2CO3 (1.68 g, 12.24 mmol) and methyl triphenyl phosphonium bromide (4.37 g, 12.24 mmol) at ambient temperature. Then the resultant reaction mixture was heated at 100° C. for 18 h. After the reaction was deemed complete by TLC, the reaction mixture was cooled to ambient temperature and filtered, and the obtained filtrate was concentrated under reduced pressure. The residue was purified by flash chromatography (SiO2, 100-200 mesh; 20% EtOAc in n-Hexane) to afford the title compound as a white solid (1.94 g, 70%): mp 141-143° C.; 1H NMR (400 MHz, CDCl3) δ 7.85 (m, 2H), 7.70 (m, 2H), 7.41 (m, 1H), 7.21 (m, 2H), 6.71 (dd, J=17.6, 10.8 Hz, 1H), 5.72 (d, J=17.6 Hz, 1H), 5.23 (d, J=10.8 Hz, 1H), 4.92 (s, 2H); ESIMS m/z 298.10 ([M−H]−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212163B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-88f54c8ac83b4ca38a7090cede9194a2 |
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| Source note | uspto-grants-2015_12 |
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