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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372932Generated: October 30, 2026

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

https://huagongshe.com/reaction/372932

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 numberUS05160662
Source datasetuspto-grants-1992_11
ORD IDord-3cdbc7495be245c7b1444aba18c1824c
Source noteuspto-grants-1992_11