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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DifluoroanilineHCID 9709—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-Bromobutyric acidHCID 75809—
SolventDimethylformamideHCID 6228—
Product4-bromo-N-(2,4-difluorophenyl)butanamideHCID 2263353158%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825223B2
Source datasetuspto-grants-2004_11
ORD IDord-b62791565c424893b8317f26391ad3a3
Source noteuspto-grants-2004_11