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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984882Generated: November 1, 2026

Hydrochloric Acid → 4-Bromo-2-(trifluoromethoxy)benzoic acid

https://huagongshe.com/reaction/1984882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfamic AcidHCID 5987—
ReactantSodium CarbonateHCID 10340—
Reactant4-Bromo-2-(trifluoromethoxy)benzaldehydeHCID 18700087—
ReactantSodium ChloriteHCID 23668197—
ReactantSodium Phosphate, Monobasic, DihydrateHCID 23673460—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product4-Bromo-2-(trifluoromethoxy)benzoic acidHCID 1666557281%

Reaction Conditions

Temperature4 °C

Reaction Steps

A solution of 4-bromo-2-trifluoromethoxy-benzaldehyde (550 mg, 2.04 mmol) in 1,4-dioxane (27 mL) and H2O (9 mL) was cooled at 4° C. To the solution were added amidosulfuric acid (296 mg, 3.05 mmol) and sodium dihydrogen phosphate dihydrate (1.4 g, 8.98 mmol). The mixture was stirred at 4° C. for 15 min. To the reaction mixture was added a solution of sodium chlorite (238 mg, 2.63 mmol) in H2O (1.5 mL) and stirred at 4° C. for 15 min. To the reaction mixture was added Na2CO3 (304 mg, 2.41 mmol) and stirred at 4° C. for 15 min. The mixture was acidified with conc-HCl (pH=1), and the aqueous layer was extracted with CHCl3 (three times). The combined organic layer was dried over MgSO4, filtered, concentrated, and purified by flash chromatography (silica gel, 1% MeOH in CHCl3) to give 4-bromo-2-trifluoromethoxy-benzoic acid (471 mg, 81%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544690B2
Source datasetuspto-grants-2009_06
ORD IDord-229d4df18a5f4f82bc7e229e9dc16474
Source noteuspto-grants-2009_06