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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042730Generated: October 27, 2026

Triethylamine → 3-bromo-4-fluoro-N-(2-fluoro-3-(trifluoromethyl)phenyl)benzamide

https://huagongshe.com/reaction/1042730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Bromo-4-fluorobenzoyl chlorideHCID 69598—
Reactant3-Amino-2-fluorobenzotrifluorideHCID 145569—
SolventDichloromethaneHCID 6344—
Product3-bromo-4-fluoro-N-(2-fluoro-3-(trifluoromethyl)phenyl)benzamideHCID 59427998—

Reaction Steps

2-Fluoro-3-(trifluromethyl)aniline (0.515 g, 0.37 mL, 2.88 mmol) was added to a solution of 3-bromo-4-fluorobenzoyl chloride (0.650 g, 2.74 mmol) in dichloromethane (5 ml), and the mixture stirred at room temperature for 30 min. Triethylamine (0.360 g, 0.50 ml, 3.56 mmol) was added and the solution stirred at room temperature for 1 h. The reaction mixture was partitioned between dichloromethane and saturated aqueous sodium bicarbonate solution. The aqueous phase was separated and extracted with dichloromethane. The combined organic phases were washed with water, brine, dried over anhydrous sodium sulfate, filtered, and concentrated to afford a light yellow solid. Trituration with dichloromethane and filtering afforded 3-bromo-4-fluoro-N-(2-fluoro-3-(trifluoromethyl)phenyl)benzamide as a white solid. MS (M−H+) 377.9; Calculated for C14H7BrF5NO: 379.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557996B2
Source datasetuspto-grants-2013_10
ORD IDord-65ca380cbc5240f69c22d949f24214c8
Source noteuspto-grants-2013_10