HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564446Generated: October 30, 2026
Dimethylformamide → 2-[(3-bromo-5-methylphenyl)methyl]-1H-isoindole-1,3(2H)-dione
https://huagongshe.com/reaction/564446
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Bromo-3-(bromomethyl)-5-methylbenzene | HCID 22324261 | — |
| Reactant | Potassium phthalide | HCID 67006573 | — |
| Product | 2-[(3-bromo-5-methylphenyl)methyl]-1H-isoindole-1,3(2H)-dione | HCID 57813441 | 67% |
Reaction Steps
To a solution of 1-bromo-3-(bromomethyl)-5-methylbenzene (34.0 g, 128.8 mmol) in DMF (200 mL), was added potassium phthalide (28.9 g, 154.6 mmol), and the mixture was stirred under reflux for 2 h. The reaction was allowed to cool to room temperature. After the solvent was remove under reduced pressure, the residue was dissolved in CH2Cl2 (300 mL), and washed with water (50 mL×3). The organic layer was dried over anhydrous sodium sulfate. Evaporation of the solvent gave a white solid. The solid was recrystallized from toluene and EtOH to give the product, 2-[(3-bromo-5-methylphenyl)methyl]-1H-isoindole-1,3(2H)-dione (28.5 g, 67%). 1H NMR (400 MHz, CDCl3): δ 7.87-7.72 (m, 4 H), 7.36 (s, 1H), 7.23 (s, 1 H), 7.15 (s, 1 H), 4.77 (s, 2 H), 2.30 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08067408B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-d3361df022ff41b998f0dc64a9effee9 |
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| Source note | uspto-grants-2011_11 |
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