HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929379Generated: November 1, 2026
Aniline → 3,4-Dibromo-1-phenyl-1H-pyrrole-2,5-dione
https://huagongshe.com/reaction/929379
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aniline | HCID 6115 | — |
| Reactant | 2,5-Furandione, 3,4-dibromo- | HCID 70727 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3,4-Dibromo-1-phenyl-1H-pyrrole-2,5-dione | HCID 13059268 | 63.7% |
Reaction Steps
Aniline (72 μL, 0.788 mmol) was added to a solution of dibromomaleic anhydride (200 mg, 0.788 mmol) in AcOH (10 mL). The mixture was stirred for 3 h at RT and at 130° C. for 90 mins. After cooling, the mixture was concentrated to dryness and traces of AcOH removed by azeotrope with toluene. The tan residue was purified using silica flash chromatography (5% EtOAc/95% petroleum ether) to yield the desired compound as a pale yellow solid (166 mg, 60%). δH (600 MHz, CDCl3) 7.48 (m, 2H, ArH), 7.41 (tt, 1H, J=7.4 and 1.1 Hz, ArH), 7.33 (m, 2H, ArH); δC (150 MHz, CDCl3) 163.0, 131.0, 130.0, 129.5, 128.8, 126.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09295729B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-a55630c50e2e445baf781239712b64d1 |
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| Source note | uspto-grants-2016_03 |
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