HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416951Generated: October 27, 2026
2,4-Difluoroaniline → 4-bromo-N-(2,4-difluorophenyl)butanamide
https://huagongshe.com/reaction/2416951
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4-Difluoroaniline | HCID 9709 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 4-Bromobutyric acid | HCID 75809 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-bromo-N-(2,4-difluorophenyl)butanamide | HCID 22633531 | 58% |
Reaction Steps
WSC (2.1 g, 11 mmols) and HOBt (1.49 g, 11 mmols) were added to a DMF (30 ml) solution of 2,4-difluoroaniline (1.29 g, 10 mmols) and 4-bromobutyric acid (2.5 g, 15 mmols), and stirred at room temperature for 12 hours. The reaction mixture was extracted with ether. The organic layer was washed with water 1 N HCl, an aqueous saturated solution of sodium hydrogencarbonate and saturated saline in that order, and dried with anhydrous magnesium sulfate, and the solvent was evaporated. Then, the residue was purified through preparative thin-layer chromatography (developer:hexane/acetone=5/1), and the resulting crystals were recrystallized from ether-hexane to obtain 1.6 g (yield: 58%) of 4-bromo-N-(2,4-difluorophenyl)butanamide as colorless needle-like crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06825223B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-b62791565c424893b8317f26391ad3a3 |
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| Source note | uspto-grants-2004_11 |
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