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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868461Generated: October 25, 2026

Hydrochloric Acid → 2-Methyl-5(2-chloro-4-trifluoromethylphenoxy)-benzoic acid

https://huagongshe.com/reaction/868461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant4-Hydroxy-o-toluic acidHCID 68475—
ReactantBenzene, 2-chloro-1-fluoro-4-(trifluoromethyl)-HCID 157153—
SolventWaterHCID 962—
Product2-Methyl-5(2-chloro-4-trifluoromethylphenoxy)-benzoic acidHCID 21287066—

Reaction Steps

A mixture of sodium hydride (2.3 g, 50% dispersion in mineral oil, prewashed with petroleum, b.p. 40°-60°) and 4-hydroxy-2-methylbenzoic acid (3.4 g) in dry N,N-dimethylformamide (30 ml) was stirred for thirty minutes, then treated with 3-chloro-4-fluorobenzotrifluoride (4.5 g). The mixture was heated at 130° for five hours, cooled, diluted with water, acidified with 2N hydrochloric acid and extracted with ethyl acetate. The extracts were washed with water and brine, dried and evaporated. The residue was recrystallised from petroleum (b.p. 80°-100°) to give 2-methyl-5(2-chloro-4-trifluoromethylphenoxy)-benzoic acid (2.06 g, m.p. 113°). A suspension of this material (1.34 g) in thionyl chloride (5 ml) was heated under reflux for one hour and the excess reagent removed in vacuo. The residue was dissolved in acetonitrile and again evaporated to give crude acid chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04780128
Source datasetuspto-grants-1988_10
ORD IDord-f7194b03cabf4d6180b3f0d57e13a1c6
Source noteuspto-grants-1988_10