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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358196Generated: October 29, 2026

3-Hydroxybenzoic Acid → 3(2-Chloro-5-trifluoromethylphenoxy)benzoic acid

https://huagongshe.com/reaction/358196

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Hydroxybenzoic AcidHCID 7420—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Chloro-3-fluorobenzotrifluorideHCID 2736545—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3(2-Chloro-5-trifluoromethylphenoxy)benzoic acidHCID 1938925056.9%

Reaction Steps

3-Hydroxybenzoic acid (3.45 g) was added to a solution of potassium hydroxide (2.8 g) in methanol. The solution was evaporated under reduced pressure to give a white solid. This was taken up in dry dimethylsulphoxide (25 ml). The resulting solution was stirred and heated at 170° with anhydrous potassium carbonate (1.25 g) and 4-chloro-3-fluorobenzotrifluoride (5 g) for 12 hours. The mixture was then cooled and poured into water, (500 ml). The mixture was extracted with ether and then acidified (HCl). The precipitate which formed was recrystallised from petroleum (b.p. 60°-80°) to give the required acid (4.5 g) with a melting point of 142°-143°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04465508
Source datasetuspto-grants-1984_08
ORD IDord-4c414571f23a41c0bc1fbec9940b552e
Source noteuspto-grants-1984_08