Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50502Generated: October 26, 2026

1-(4-Fluorophenoxy)-3-nitrobenzene → 3-(4-Fluorophenoxy)aniline

https://huagongshe.com/reaction/50502

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Fluorophenoxy)-3-nitrobenzeneHCID 23506030—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-(4-Fluorophenoxy)anilineHCID 2350601591.8%

Reaction Steps

EX-634B) 3-(4Fluorophenoxy)nitrobenzene (1.15 g, 4.93 mmol) from EX-634A was dissolved in ethanol (45 mL), and the solution was hydrogenated for 4 h in the presence of 5% palladium on charcoal. After the mixture was filtered through celite, the ethanol was removed in vacuo. The product was purified by flash column chromatography on silica gel eluting with ethyl acetate in hexane (1:10) to give 0.92 g (90%) of 3-(4-fluorophenoxy)aniline as a yellow oil, 99% pure by HPLC analysis. HRMS calcd. for C12H11FNO: 204.0824 [M+H]+, found: 204.0837.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710089B2
Source datasetuspto-grants-2004_03
ORD IDord-899a0c6dd93e4de19bcc96b450700d3d
Source noteuspto-grants-2004_03