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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968931Generated: November 1, 2026

4-Methyl-3-(trifluoromethyl)benzoic acid → 4-(Bromomethyl)-3-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/1968931

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-3-(trifluoromethyl)benzoic acidHCID 2775592—
ReactantSodium BisulfiteHCID 23665763—
ReactantSodium BromateHCID 23668195—
SolventIsopropyl AcetateHCID 7915—
Product4-(Bromomethyl)-3-(trifluoromethyl)benzoic acidHCID 23145893—

Reaction Steps

1.0 g of 4-methyl-3-(trifluoromethyl)benzoic acid was dissolved in isopropyl acetate (q.s.). To the mixture, sodium bromate aqueous solution (10 ml, containing 2.2 g of sodium bromate) and sodium bisulfite aqueous solution (10 ml, containing 1.52 g of sodium bisulfite) were added alternatively with stirring. After addition, the solution became brownish red. The mixture was heated to reflux until the solution became colorless. Then the organic layer was separated. Again, to the mixture, sodium bromate aqueous solution (10 ml, containing 2.2 g sodium bromate) and sodium bisulfite aqueous solution (10 ml, containing 1.52 g sodium bisulfite) were added alternatively and the mixture was heated to reflux until the solution became colorless. Then the organic layer was separated. Continually, to the mixture, a sodium bromate aqueous solution (10 ml, containing 2.2 g sodium bromate) and a sodium bisulfite aqueous solution (10 ml, containing 1.52 g sodium bisulfite) were added alternatively, and the mixture was heated to reflux until the solution became colorless. Then the organic layer was separated. The organic layer was washed with 5% sodium sulfate solution twice and 15% sodium chloride solution twice, dried over anhydrous Na2SO4, filtered, concentrated under reduced pressure to dry. The is residue was stirred in petroleum ether, and filtered to give a white solid. m.p. 140-145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426446B2
Source datasetuspto-grants-2013_04
ORD IDord-9c45df9794e847b1bb1519d14107bcf8
Source noteuspto-grants-2013_04