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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439549Generated: October 26, 2026

Acetic Acid → 2-Bromo-4-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/439549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrogen BromideHCID 260—
Reactant4-(Trifluoromethyl)anthranilic acidHCID 67869—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product2-Bromo-4-(trifluoromethyl)benzoic acidHCID 6760580%

Reaction Conditions

Temperature-10 °C

Reaction Steps

205 g (1 mol) of 4-(trifluoromethyl)anthranilic acid, 600 ml of glacial acetic acid and 400 ml of 47% hydrobromic acid are introduced successively into a three-liter round-bottomed flask. After dissolution, the reaction mixture is cooled to -10° C., diluted with 400 ml of water and then treated dropwise with a solution of 69 g (1 mol) of sodium nitrite in 200 ml of water while maintaining the temperature below 0° C. When the addition is finished, the reaction mixture is stirred at 0° C. for 2 hours. This solution is run in dropwise into a six-liter reactor containing 143.5 g (1 mol) of cuprous bromide in 500 ml of 47% hydrobromic acid maintained at 60° C. When the addition is finished, the reaction mixture is stirred at 60° C. for one hour, cooled to room temperature and then poured into two liters of ice-cold water. The precipitate which forms is filtered on sintered glass, washed with water and then dried under a stream of air. There is thus obtained 216 g (yield: 80%) of 2-bromo-4-(trifluoromethyl)benzoic acid in the form of a solid melting at 118.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05514719
Source datasetuspto-grants-1996_05
ORD IDord-593f390d21b44bd0bfa3e3cbbd0b2b3d
Source noteuspto-grants-1996_05