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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036179Generated: October 26, 2026

Hydrochloric Acid → 4-Bromo-3-(trifluoromethyl)benzeneacetic acid

https://huagongshe.com/reaction/1036179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfuric AcidHCID 1118—
ReactantSodium CarbonateHCID 10340—
Reactant4-Bromo-3-(trifluoromethyl)phenylacetonitrileHCID 45933702—
SolventWaterHCID 962—
Product4-Bromo-3-(trifluoromethyl)benzeneacetic acidHCID 26986360—

Reaction Conditions

Temperature115 °C

Reaction Steps

To a flask containing 2-(4-bromo-3-(trifluoromethyl)phenyl)acetonitrile 46-5 (880 mg, 3.3 mmol) were added water (4.5 mL) and dropwise concentrated sulfuric acid (4.5 mL). The reaction mixture was stirred at 115° C. for 4 hours. After cooled down to room temperature, the reaction mixture was poured into water (100 mL). The resulting solution was neutralized with powder sodium carbonate to pH 12, treated with 1N HCl aqueous solution to pH around 2, and extracted with dichloromethane (50 mL×3). The combined organic layers were washed with brine, dried over Na2SO4 and then taken to dryness by rotary evaporation give 2-(4-bromo-3-(trifluoromethyl)phenyl)acetic acid 46-6 as pale yellow solid. MS m/z 283.1 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546396B2
Source datasetuspto-grants-2013_10
ORD IDord-0e866bc48040422a95b9564aa1279754
Source noteuspto-grants-2013_10