Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270790Generated: October 26, 2026

Hydrochloric Acid → 2-Iodo-5-(trifluoromethoxy)benzoic acid

https://huagongshe.com/reaction/1270790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
Reactant2-amino-5-(trifluoromethoxy)benzoic AcidHCID 11085349—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product2-Iodo-5-(trifluoromethoxy)benzoic acidHCID 18451532—

Reaction Conditions

Temperature0 °C

Reaction Steps

The above 5-trifluoromethoxyanthranilic acid (68.8 g, 0.31 mol) is suspended in a mixture of concentrated HCl (50 mL) and water (300 mL), cooled to 0° C. and stirred. Sodium nitrite (24.2 g 0.35 mol) dissolved in water (50 mL) is slowly added taking care to maintain the temperature of the reaction mixture below 5° C. Stirring is continued at 0° C. for 30 minutes. Potassium iodide (91 g, 0.55 mol) is dissolved in a mixture of concentrated H2SO4 (19 mL) and water (130 mL) and added dropwise to the reaction mixture while keeping the temperature of the reaction mixture below 10° C. The mixture is then heated to 100° C. and stirred for 2 hours. After cooling to room temperature, the mixture is partitioned between EtOAc (1000 mL) and saturated sodium bisulfite solution (500 mL). The organic layer is washed again with saturated sodium bisulfite solution (500 mL) and then brine (500 mL), dried (MgSO4) and concentrated by rotary evaporator to give 5-trifluoromethoxy-2-iodobenzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202364B2
Source datasetuspto-grants-2007_04
ORD IDord-4cc4eebe56ef433d90a13a3fd38e5cf1
Source noteuspto-grants-2007_04