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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894928Generated: October 29, 2026

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

https://huagongshe.com/reaction/894928

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-cyano-benzotrifluoride (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 numberUS04285723
Source datasetuspto-grants-1981_08
ORD IDord-72ccb4973dd04c44a67b9b72b486d370
Source noteuspto-grants-1981_08