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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448198Generated: October 31, 2026

3-(Trifluoromethyl)phenol → Halofenate

https://huagongshe.com/reaction/448198

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 numberUS08481597B2
Source datasetuspto-grants-2013_07
ORD IDord-6b6cfca69d38484e8bd5d0da33f6c804
Source noteuspto-grants-2013_07