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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant4-Nitro-1-(4-trifluoromethoxyphenoxy)-2-trifluoromethylbenzeneHCID 86094922—
ReactantSodium bicarbonate waterHCID 86585896—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
Product4-(4-Trifluoromethoxyphenoxy)-3-trifluoromethylanilineHCID 8609486799.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880006B2
Source datasetuspto-grants-2011_02
ORD IDord-a8229b671f1549b48309640ce674f7ee
Source noteuspto-grants-2011_02