HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387080Generated: November 1, 2026
Water → 2-(4-Bromo-2-ethyl-benzyl)-isoindole-1,3-dione
https://huagongshe.com/reaction/2387080
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Reactant | 4-Bromo-1-(bromomethyl)-2-ethylbenzene | HCID 58764075 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-Bromo-2-ethyl-benzyl)-isoindole-1,3-dione | HCID 58764287 | — |
Reaction Steps
To 4-bromo-1-bromomethyl-2-ethyl-benzene (4.0 g, 14.2 mmol) in dimethylformamide (100 mL) at room temperature was added potassium phthalimide (2.9 g, 15.6 mmol), and the solution was heated at 80° C. for 5 h. The solution was cooled to room temperature and poured into water. The aqueous solution was extracted with ethyl acetate. The pooled organics were washed with saturated sodium chloride, dried (Na2SO4), filtered, and concentrated in vacuo to a yellow solid (4.0 g, 82%). 1H NMR (300 MHz, CDCl3): δ ppm 1.27 (t, J=7.54 Hz, 3 H) 2.85 (q, J=7.60 Hz, 2 H) 4.84 (s, 2 H) 7.14-7.18 (m, 1 H) 7.24-7.27 (m, 1 H) 7.34 (d, J=2.07 Hz, 1 H) 7.73 (dd, J=5.46, 3.01 Hz, 2 H) 7.86 (dd, J=5.56, 3.11 Hz, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08268835B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-bb1807c710244abfb8bacd13278b19ee |
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| Source note | uspto-grants-2012_09 |
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