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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466817Generated: October 30, 2026

2-Fluoroaniline → 4-Bromo-2-fluoroaniline

https://huagongshe.com/reaction/466817

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoroanilineHCID 9584—
Reactant4-FluoroanilineHCID 9731—
ReactantBromineHCID 24408—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventFluorobenzeneHCID 10008—
Product4-Bromo-2-fluoroanilineHCID 123050—

Reaction Steps

In a suitable aprotic solvent (e.g., CH2Cl2, toluene, fluorobenzene, or the like) 1 mole of tetrabutylammonium bromide is dissolved and stirred as 1 mole of Br2 (bromine) is added. This mixture of tetrabutylammonium trihalide and solvent is cooled to 10° before 1 mole of 2-fluoroaniline or 4-fluoroanilin, or a mixture of both, is added. The reaction takes place immediately to produce 4-bromo-2-fluoroaniline.HBr, or 2-bromo-4-fluoroaniline.HBr, or a mixture of the two. The salt is then collected and dried before carrying it up to the next step. Catalyst and solvent are recovered for recycle.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05157169
Source datasetuspto-grants-1992_10
ORD IDord-3cd2bd1330394cf9866198f7366292b2
Source noteuspto-grants-1992_10