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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897885Generated: October 30, 2026

4-Bromoaniline → HCID 22346912, compound

https://huagongshe.com/reaction/897885

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. 1H NMR (DMSO-d6, 400 MHz) δ 10.74 (s, 1H), 7.90 (m, 2H), 7.74 (d, 1H), 7.68 (d, 2H), 7.56 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921763B2
Source datasetuspto-grants-2005_07
ORD IDord-2b9b5d8870e54862b9e7c31952d84f77
Source noteuspto-grants-2005_07