HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587723Generated: October 29, 2026
4-(Bromomethyl)-1-naphthaldehyde → 4-((1,3-Dioxoisoindolin-2-yl)methyl)-1-naphthaldehyde
https://huagongshe.com/reaction/587723
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(Bromomethyl)-1-naphthaldehyde | HCID 10911903 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-((1,3-Dioxoisoindolin-2-yl)methyl)-1-naphthaldehyde | HCID 86675187 | 99.7% |
Reaction Steps
To a stirred solution of 4-(bromomethyl)-1-naphthaldehyde (7 g, 28 mmol) in DMF (100 mL) was added potassium phthalimide (7.3 g, 39.5 mmol), and the mixture was heated at 85° C. for 2 h. The reaction mixture was cooled to ambient temperature and diluted with water (100 mL). The obtained solid was separated by filtration and dried under vacuum to afford the title compound as a white solid (8.8 g, 98%): mp 190-192° C.; 1H NMR (400 MHz, CDCl3) δ 10.39 (s, 1H), 9.25 (m, 1H), 8.41 (m, 1H), 8.10 (d, J=8.0 Hz, 1H), 7.95 (m, 4H), 7.80 (m, 4H), 7.61 (m, 4H), 5.39 (s, 2H); ESIMS m/z 316.09 ([M+H]+); IR (thin film) 1708 cm−1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09226501B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-3f8ccc92d2714f92a68944ca35c8dbf0 |
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| Source note | uspto-grants-2016_01 |
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