HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238311Generated: October 25, 2026
Dimethylformamide → 2-[3-(4-Fluoro-2-nitrophenoxy)propyl]isoindole-1,3-dione
https://huagongshe.com/reaction/238311
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-3-Bromopropylphthalimide | HCID 21611 | — |
| Reactant | 4-Fluoro-2-nitrophenol | HCID 136236 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[3-(4-Fluoro-2-nitrophenoxy)propyl]isoindole-1,3-dione | HCID 66917158 | 100.4% |
Reaction Steps
Potassium carbonate (10.8 g, 78.1 mmol) and N-(3-bromopropyl)phthalimide (12.1 g, 45.1 mmol) were added to a N,N-dimethylformamide (DMF) solution (80 ml) of 4-fluoro-2-nitrophenol (6.0 g, 38.2 mmol), and the mixture was stirred at 60° C. for 4 hours. After the reaction mixture was cooled to room temperature, water (200 ml) was added, and the reaction mixture was then cooled with ice. The precipitated insoluble matter was collected by filtration. After being washed with water (50 ml×3), the substance remaining in the filter was air-dried, giving 13.2 g of powdery pale yellow 2-[3-(4-fluoro-2-nitrophenoxy)propyl]isoindole-1,3-dione (yield: 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642619B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-eac80c56130c4a7aa034e5f0c148058a |
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| Source note | uspto-grants-2014_02 |
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