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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879912Generated: October 30, 2026

Bromobenzene → 2-chloro-4-fluoro-N-phenylaniline

https://huagongshe.com/reaction/879912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantBenzenamine, 2-chloro-4-fluoro-HCID 75013—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
SolventO-XyleneHCID 7237—
Product2-chloro-4-fluoro-N-phenylanilineHCID 8605114944%

Reaction Steps

A mixture of 35 g (240 mmole) 2-chloro-4-fluoroaniline, 37.7 g (240 mmole) of bromobenzene, 0.6 g (12 mmole) of palladium (II)acetate, 4.8 g (24 mmole) of tri-tert-butylphosphine, 46 g (480 mmole) of sodium tert-butoxide and o-xylene 800 ml were refluxed under nitrogen for about overnight. Then, the solution was filtered at 100° C. To receive the filtrate, And the o-xylene was removed under reduced pressure from the filtrate. The filtrate was extracted with 500 ml dichloromethane and 2000 ml water, the organic layer was dried with anhydrous magnesium sulfate, the solvent was removed and the residue was purified by column chromatography on silica (hexane-ethyl acetate) to give product 23.4 g (44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993130B2
Source datasetuspto-grants-2015_03
ORD IDord-18d148fb42554e4b89a7bcf6d9cb2e59
Source noteuspto-grants-2015_03