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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898005Generated: October 29, 2026

4-Bromoaniline → HCID 22346912, compound

https://huagongshe.com/reaction/898005

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanilineHCID 7807—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Fluoro-4-(trifluoromethyl)benzoyl chlorideHCID 145580—
SolventDichloromethaneHCID 6344—
ProductHCID 22346912HCID 2234691287.9%

Reaction Steps

A solution of 2-fluoro-4-(trifluoromethyl)benzoyl chloride (5.05 g, 0.0223 mol) and 4-bromoaniline (3.83 g, 0.0223 mol) in anhydrous dichloromethane (150 mL) was cooled to 0° C. and N,N-diisopropylethylamine (4.26 mL, 0.0245 mol) was added under nitrogen atmosphere dropwise. The resulting mixture was stirred at ambient temperature for 24 hours, concentrated and the residue was partitioned between ethyl acetate (120 mL) and water (100 mL). The organic phase was washed with brine, dried with magnesium sulfate and concentrated. The residue was suspended in cold n-heptane (50 mL) and the precipitate was collected by filtration and dried to yield N1-(4-bromophenyl)-2-fluoro-4-(trifluoromethyl)benzamide (7.1 g, 0.0196 mol) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921763B2
Source datasetuspto-grants-2005_07
ORD IDord-56661b40f46b48359412f14f62c72dd5
Source noteuspto-grants-2005_07