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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586019Generated: October 26, 2026

Hydrogen Bromide → 3-Bromo-4-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/586019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantUreaHCID 1176—
ReactantSodium HydroxideHCID 14798—
Reactant3-Amino-4-(trifluoromethyl)benzoic acidHCID 642651—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product3-Bromo-4-(trifluoromethyl)benzoic acidHCID 22337570—

Reaction Conditions

Temperature75 °C

Reaction Steps

3-Amino-4-trifluoromethylbenzoic acid (8.20 g, 40.0 mmol), prepared according to Astrid Giencke and Helmut Lackner, Liebigs Ann. Chem., 569-579:6 (1990), in 48% HBr (20 mL) and H2O (67 mL) at 0° C. was treated with NaNO2 (2.99 g) in small portions over 15 minutes. After stirring for 30 minutes, the mixture was treated with urea (0.250 g) and then the mixture was added dropwise to a solution of CuBr (10.0 g) in 48% HBr (40 mL) and H2O (100 mL). The reaction mixture was heated at 75° C., stirred for 2 hours, cooled to room temperature, and stirred overnight. The mixture was treated with with 20% NaOH until the pH>10. The resulting blue copper salts were removed by filtration through Celite. The mixture was acidified to pH 1 with HCl, extracted with CH2Cl2 (3×200 mL), dried over Na2SO4, filtered, and the filtrate was concentrated under reduced pressure to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06933311B2
Source datasetuspto-grants-2005_08
ORD IDord-009882c007344d3aab7baa74d8e1f325
Source noteuspto-grants-2005_08