HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917541Generated: October 31, 2026
1-Bromo-3-(bromomethyl)-5-chlorobenzene → 2-(3-Bromo-5-chlorobenzyl)isoindoline-1,3-dione
https://huagongshe.com/reaction/917541
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-3-(bromomethyl)-5-chlorobenzene | HCID 22324264 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(3-Bromo-5-chlorobenzyl)isoindoline-1,3-dione | HCID 58962950 | 85.6% |
Reaction Steps
Step G3. A mixture of 1-bromo-3-(bromomethyl)-5-chlorobenzene (6 g, ˜21 mmol) and potassium phthalimide (3.15 g, 17 mmol) in DMF (50 ml) was heated at 120° C. for 2 hours. After cooled down, a white solid precipitated. The solid was filtered and washed with ethanol, then dried in vacuum. 2-(3-Bromo-5-chlorobenzyl)isoindoline-1,3-dione (5.1 g, 85%) was obtained as white solid. 1H NMR (DMSO-d6): δδ3.72 (s, 2H), 7.43 (s, 1H), 7.51 (s, 1H), 7.52 (s, 1H), 7.84, 7.86 (d, 2H), 8.05, 8.07 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07273882B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-6b1bad60a5f840f3ac7055b20ffabba2 |
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| Source note | uspto-grants-2007_09 |
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