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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843629Generated: October 29, 2026

Benzyl Bromide → Dibenzyl-(2,4-difluoro-phenyl)-amine

https://huagongshe.com/reaction/1843629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant2,4-DifluoroanilineHCID 9709—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
ProductDibenzyl-(2,4-difluoro-phenyl)-amineHCID 58086650—

Reaction Steps

To 2,4-difluoroaniline (40.0 g, 0.31 mol) in N,N-dimethylformamide (400 mL) were added potassium carbonate (120 g, 0.92 mol, 3 eq) and benzyl bromide (112 mL, 0.71 mmol, 2.3 eq). The reaction was stirred with mechanical stirring at room temperature overnight. In order to quench the benzyl bromide in excess, NH4OH (90 mL) was added and the reaction was stirred overnight. The mixture was filtered and DMF was evaporated under reduced pressure. Ethyl acetate was added and the organic layer was washed with water and brine, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure and the oily crude was crystallized in methanol, obtaining after drying 71 g of dibenzyl-(2,4-difluoro-phenyl)-amine as a white solid (74%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946250B2
Source datasetuspto-grants-2015_02
ORD IDord-2460358f766447d59a4852440ec12140
Source noteuspto-grants-2015_02