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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168465Generated: October 28, 2026

3-(Trifluoromethyl)phenol → Halofenate

https://huagongshe.com/reaction/1168465

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)phenolHCID 7376—
ReactantPotassium HydroxideHCID 14797—
Reactant2-(Acetylamino)ethyl α-bromo-4-chlorobenzeneacetateHCID 22025314—
ReactantHCID 131724051HCID 131724051—
SolventIsopropanolHCID 3776—
ProductHalofenateHCID 33584—

Reaction Steps

3-Hydroxybenzotrifluoride was added to a solution of potassium hydroxide in isopropanol. N-acetylaminoethyl 2-bromo-2-(4-chlorophenyl)acetate in isopropanol was added to the isopropanol/phenoxide solution and stirred at room temperature for 4 hours. The isopropanol was removed by vacuum distillation, and the resulting slush was dissolved in ethyl acetate and washed twice with water and once with brine. After drying over magnesium sulfate and filtration, the solvent was removed to give crude product as an oil. The crude product was dissolved in hot toluene/hexanes (1:1 v/v) and cooled to between 0 and 10° C. to crystallize the product. The filter cake was washed with hexanes/toluene (1:1 v/v) and then dried under vacuum at 50° C. The isolated solid was dissolved in hot 1:6 (v/v) isopropanol in hexanes. After cooling, the pure racemic 2-Acetamidoethyl 4-Chlorophenyl-(3-trifluoro methylphenoxy)-acetate formed as a crystalline solid. The solid was collected by filtration, the filter cake washed with 1:6 (v/v) isopropanol in hexanes and dried under vacuum at 50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06624194B1
Source datasetuspto-grants-2003_09
ORD IDord-158332137e2948a78391fd3efe5c2c0c
Source noteuspto-grants-2003_09