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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374850Generated: October 30, 2026

Benzyl Bromide → N-benzyl-4-fluoroaniline

https://huagongshe.com/reaction/1374850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantTriethylamineHCID 8471—
Reactant4-FluoroanilineHCID 9731—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductN-benzyl-4-fluoroanilineHCID 91340246%

Reaction Steps

A solution of 4-fluoroaniline (1.50 g, 13.5 mmol)and triethylamine (2.26 mL, 16.2 mmol) in dichloromethane (7 mL) was cooled to 0° C., and the solution was added dropwise with benzyl bromide (1.61 mL, 13.5 mmol). After stirring at room temperature for 1 hour, the reaction mixture was diluted with ethyl acetate and washed three times with water and then with brine, and dried over Na2SO4. The drying agent was removed by filtration and the filtrate was concentrated, the residue was purified by silica gel chromatography (ethyl acetate/hexane) to obtain the title compound (yield: 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166617B2
Source datasetuspto-grants-2007_01
ORD IDord-cf15c83cb22a40deb7cb91c533131ed7
Source noteuspto-grants-2007_01