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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679241Generated: October 31, 2026

4-Aminophenol → 4-[2,6-Dichloro-4-(trifluoromethyl)phenoxy]aniline

https://huagongshe.com/reaction/1679241

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
ReactantPotassium HydroxideHCID 14797—
Reactant1,2,3-Trichloro-5-(trifluoromethyl)benzeneHCID 2733399—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product4-[2,6-Dichloro-4-(trifluoromethyl)phenoxy]anilineHCID 20362097—

Reaction Steps

32.5 g of potassium hydroxide flakes in 30 ml of water were added to 54.5 g (0.5 mole) of 4-aminophenol dissolved in 350 ml of dimethylsulfoxide, and 150 ml of a water/dimethylsulfoxide mixture were distilled off in vacuo at 15-20 mm Hg. 125 g (0.5 mole) of 1-trifluoromethyl-3,4,5-trichlorobenzene [nD20 : 1.5008 67- 68% of theory, compare J. Am. Chem. Soc. 57, 2066-2068 (1935) and U.S. Pat. No. 2,654,789] were then added to the reaction mixture at about 70°-80° C and the mixture was stirred for a further 2 hours at 120°-130° C. The substance was precipitated with water, filtered off, washed with water and recrystallized moist from an ethanol/water mixture, thus giving 40-50% of theory of 4-(2,6-dichloro-4-trifluoromethylphenoxy)-aniline of melting point 128°-130° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04080193
Source datasetuspto-grants-1978_03
ORD IDord-9f7380e6b30646d6b675cb3377376abe
Source noteuspto-grants-1978_03