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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193983Generated: October 25, 2026

Hydrochloric Acid → 3-Chloro-2-fluoro-5-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/2193983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantSodium SulfiteHCID 24437—
ReactantSodium BromideHCID 253881—
Reactant3-Chloro-2-fluoro-5-(trifluoromethyl)benzaldehydeHCID 736336—
ReactantSodium HypochloriteHCID 23665760—
SolventWaterHCID 962—
SolventCyclohexaneHCID 8078—
Product3-Chloro-2-fluoro-5-(trifluoromethyl)benzoic acidHCID 277375170.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

To an aqueous solution of sodium hypochlorite (15.3 ml, 25.7 mmol, 1.2 equiv.) and sodium bromide (2.6 g, 25.7 mmol, 1.2 equiv.) in sodium hydroxide solution (47%, 4.55 ml, 53.5 mmol, 2.50 equiv.) and water (12.5 ml) was added slowly (during 25 min) at 50° C. 3-chloro-2-fluoro-5-trifluoromethyl-benzaldehyde (5.0 g, 21.4 mmol). The reaction mixture was stirred at 50° C. for 60 min, cooled to ambient temperature and quenched upon addition of aqueous sodium sulfite solution (20%, 16.2 ml, 25.7 mmol, 1.2 equiv.) to give a light turbid suspension. The suspension was stirred for 15 min, treated with HCl (37%, 5.0 ml, 59.1 mmol, 2.76 equiv.) adjusting the pH to 1, whereupon a white precipitate formed. This precipitate was extracted with toluene (30 ml), the organic phase was washed with brine (30 ml), whereas the aqueous phase was washed with TBME (30 ml). The combined organic phases were dried over sodium sulfate, filtered and the solvent was removed under vacuum to give the crude product as light yellow solid (5.13 g, 98.8% yield). The crude product was dissolved in hot cyclohexane (25 ml), and the solution was cooled to ambient temperature, whereupon white crystals precipitated. The crystals were filtered off, washed with cyclohexane (5 ml) dried under vacuum until weight constancy to give the title compound as white crystals (3.65 g, 69.6% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329939B2
Source datasetuspto-grants-2012_12
ORD IDord-7eaffbd04c3641ce9e7753f91acaac2b
Source noteuspto-grants-2012_12