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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842917Generated: November 1, 2026

Benzyl Bromide → HCID 70816196, compound

https://huagongshe.com/reaction/1842917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-3-fluoroanilineHCID 821848—
SolventAcetonitrileHCID 6342—
ProductHCID 70816196HCID 7081619670.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 4-bromo-3-fluoroaniline (10.0 g, 52.6 mmol, 1.0 eq) and K2CO3 (21.7 g, 157.8 mmol, 3.0 eq) in MeCN (10 mL) was added benzyl bromide (19.8 g, 115.8 mmol, 2.2 eq) and the mixture was stirred for 16 h at 80° C. and then filtered through celite pad, and the solvents was evaporated under vacuum and washed with PE (100 mL) to get N,N-dibenzyl-4-bromo-3-fluoroaniline (13.8 g, 55%; TLC system: EtOAc/PE (1:9), Rf: 0.6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946204B2
Source datasetuspto-grants-2015_02
ORD IDord-8c4865fcc9e448fa8d9057fe038d3737
Source noteuspto-grants-2015_02