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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166787Generated: November 1, 2026

3-Hydroxybenzoic Acid → 3-(2-Cyano-4-trifluoromethylphenoxy)benzoic acid

https://huagongshe.com/reaction/2166787

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Hydroxybenzoic AcidHCID 7420—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-5-(trifluoromethyl)benzonitrileHCID 67604—
SolventDimethylformamideHCID 6228—
Product3-(2-Cyano-4-trifluoromethylphenoxy)benzoic acidHCID 1301368439.1%

Reaction Steps

3-Hydroxybenzoic acid (27.6 g), 4-chloro-3-cyanobenzotrifluoride (41.1 g) and anhydrous potassium carbonate (55.2 g) were stirred together for 71/2 hours at 100° C. in dry dimethylformamide (500 ml) and then left at room temperature for 65 hours. The solvent was then removed under reduced pressure and the residue taken up in water and acidified with dilute hydrochloric acid. The solid which separated was washed with water, dissolved in ether and the solution dried and concentrated. The colourless solid which separated was recrystallised to give the benzoic acid derivative (24.0 g) with a melting point of 224°-226° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04388472
Source datasetuspto-grants-1983_06
ORD IDord-abbaba4b9187481591eee32c6ceaa497
Source noteuspto-grants-1983_06