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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439548Generated: October 26, 2026

Ethanol → Ethyl 2-bromo-4-(trifluoromethyl)benzoate

https://huagongshe.com/reaction/439548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSulfuric AcidHCID 1118—
Reactant2-Bromo-4-(trifluoromethyl)benzoic acidHCID 67605—
ProductEthyl 2-bromo-4-(trifluoromethyl)benzoateHCID 15766264100%

Reaction Steps

238 g (0.885 mol) of 2-bromo-4-(trifluoromethyl)benzoic acid, 1000 ml of absolute ethanol and 100 ml of concentrated sulfuric acid are introduced successively into a 2-liter round-bottomed flask. The reaction mixture is brought to reflux for 6 hours and then poured, after cooling, onto 2.5 liters of ice-cold water; the oil formed is extracted with ethyl acetate. The organic phase is successively washed with water, with 1N sodium hydroxide solution and then again with water. After drying over magnesium sulfate, the solvent is evaporated to provide 263 g (yield: 100%) of ethyl 2-bromo-4-(trifluoromethyl)benzoate in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05514719
Source datasetuspto-grants-1996_05
ORD IDord-bb6e42ca444748fd9e19e6039f031dd1
Source noteuspto-grants-1996_05