HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416953Generated: November 2, 2026
2,4-Difluoroaniline → HCID 22013907, compound
https://huagongshe.com/reaction/2416953
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Difluoroaniline | HCID 9709 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 10-Bromodecanoic Acid | HCID 142712 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22013907 | HCID 22013907 | 45% |
Reaction Steps
WSC (990 mg, 5.2 mmols) and HOBt (698 mg, 5.2 mmols) were added to a DMF (10 ml) solution of 2,4-difluoroaniline (1.29 g, 10 mmols) and 10-bromodecanoic acid (1.18 g, 4.7 mmols), and stirred at room temperature for 15 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 silica gel column chromatography (developer:hexane/acetone=10/1) aid the resulting crystals were recrystallized from ether-hexane to obtain 763 mg (yield, 45%) of 10-bromo-N-(2,4-difluorophenyl) decanamide 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-5c1d70fff51d452e8fea49b87e66351a |
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| Source note | uspto-grants-2004_11 |
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