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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485985Generated: October 30, 2026

p-(1-Trifluoromethylheptyloxy)nitrobenzene → p-(1-Trifluoromethylheptyloxy)-aniline

https://huagongshe.com/reaction/485985

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-(1-Trifluoromethylheptyloxy)nitrobenzeneHCID 15123947—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Productp-(1-Trifluoromethylheptyloxy)-anilineHCID 15123948—

Reaction Steps

To 100 ml of dry ethanol containing 77.7 g of oa p-(1-trifluoromethyl-heptyloxy)-nitrobenzene, was added 0.5 g of 5% Pd/C (5% palladium carbon) followed by carrying out reduction within an atmosphere of hydrogen at normal pressure under stirring at room temperature. After it was confirmed that no absorption of hydrogen was observed, the catalyst was removed by filtration and then the ethanol was distilled off to obtain 6.7 g of oily oa p-(1-trifluoromethylheptyloxy)-aniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05290478
Source datasetuspto-grants-1994_03
ORD IDord-bd92b8dd6add4baaa6f77ebbbb3a8fef
Source noteuspto-grants-1994_03