HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489788Generated: October 26, 2026
2-Butene, 1,4-dibromo- → 2-(4-Bromobut-2-en-1-yl)-1H-isoindole-1,3(2H)-dione
https://huagongshe.com/reaction/1489788
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Butene, 1,4-dibromo- | HCID 13180 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-Bromobut-2-en-1-yl)-1H-isoindole-1,3(2H)-dione | HCID 53423432 | 74% |
Reaction Steps
Potassium phthalimide (4.60 g, 24.8 mmol) was added in four portions at 15-min intervals to a solution of 1,4-dibromo-2-butene (10.60 g, 49.5 mmol) in dimethylformamide (20 mL) and the resulting mixture was stirred overnight at room temperature. The mixture was concentrated under reduced pressure and the residue was partitioned between dichloromethane (25 mL) and 2N aqueous hydrochloric acid (25 mL). The aqueous layer was-extracted with dichloromethane (2×25 mL) and the organic layers were washed in succession with saturated aqueous sodium chloride (20 mL), dried (sodium sulfate), filtered, and evaporated. The crude product was purified by flash column chromatography silica gel (150 g) eluting with 50% dichlormethane/hexane increasing to 100% dichlormethane to yield 5.12 g (74% yield) of white crystalline product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05679700 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-7e8b88c842b5499c924b83ff44c71130 |
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| Source note | uspto-grants-1997_10 |
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