HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361464Generated: October 26, 2026
Hydrochloric Acid → 4-(4-Trifluoromethoxyphenoxy)-3-trifluoromethylaniline
https://huagongshe.com/reaction/1361464
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Nitro-1-(4-trifluoromethoxyphenoxy)-2-trifluoromethylbenzene | HCID 86094922 | — |
| Reactant | Sodium bicarbonate water | HCID 86585896 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(4-Trifluoromethoxyphenoxy)-3-trifluoromethylaniline | HCID 86094867 | 99.3% |
Reaction Steps
Iron powder (72.7 g), 251 mL of ethanol, 103 mL of distilled water, and 0.55 mL of 35% hydrochloric acid were mixed together, and the mixture was heated to reflux. Subsequently, a solution of 66.9 g of 4-nitro-1-(4-trifluoromethoxyphenoxy)-2-trifluoromethylbenzene dissolved in 77 mL of ethanol was added dropwise to the mixed solution, and the mixture was heated under reflux for 2.5 hr. The reaction solution was cooled to room temperature, sodium bicarbonate water was added thereto, and the mixture was filtered. The filtrate was concentrated under the reduced pressure, and ethyl acetate and brine were added to the residue, followed by separation. The ethyl acetate layer was washed with brine and was then concentrated under the reduced pressure to give 61.0 g of 4-(4-trifluoromethoxyphenoxy)-3-trifluoromethylaniline (yield 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07880006B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-a8229b671f1549b48309640ce674f7ee |
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| Source note | uspto-grants-2011_02 |
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