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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,2,3-Trichloro-5-(trifluoromethyl)benzene | HCID 2733399 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[2,6-Dichloro-4-(trifluoromethyl)phenoxy]aniline | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04080193 |
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| Source dataset | uspto-grants-1978_03 |
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| ORD ID | ord-9f7380e6b30646d6b675cb3377376abe |
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| Source note | uspto-grants-1978_03 |
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