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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499339Generated: October 26, 2026

Hydrochloric Acid → 2-Mercapto-4-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/499339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant4-(Trifluoromethyl)anthranilic acidHCID 67869—
ReactantPotassium AcetateHCID 517044—
ReactantPotassium ethylxanthateHCID 2735045—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product2-Mercapto-4-(trifluoromethyl)benzoic acidHCID 2154213277%

Reaction Steps

A mixture of 2-amino-4-trifluoromethylbenzoic acid (5.0 g, 24 mmol), sodium hydroxide (1.0 g, 25 mmol), sodium nitrite (1.7 g, 24 mmol) and water (40 ml) was added dropwise to a mixture of concentrated hydrochloric acid (10 ml) and ice (10 g) while the reaction temperature had been kept at 0 to 5° C. The reaction mixture was stirred at the same temperature for 30 minutes, neutralized with potassium acetate and added to a solution of potassium O-ethyl dithiocarbonate (11.7 g, 73 mmol) in water (40 ml). The reaction mixture was stirred at 80° C. for 20 minutes and acidified by use of concentrated hydrochloric acid to pH 3. The water layer was separated, and the oily substance was added to 10% aqueous sodium hydroxide solution (25 g) and stirred at 80° C. for 2 hrs. Sodium hydrosulfite (3 g) was added to the mixture, and the mixture was stirred at 80° C. for 10 minutes. The reaction mixture was filtered and the filtrate was cooled and acidified by use of concentrated hydrochloric acid to pH 4. The precipitated crystals were collected by filtration, dissolved in methanol (5 ml) and diisopropylether (100 ml) and dried. The solvent was evaporated under reduced pressure to give the titled compound (4.1 g, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767665B2
Source datasetuspto-grants-2010_08
ORD IDord-53c38b8a285545ef83598286ff5c762b
Source noteuspto-grants-2010_08