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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281351Generated: November 3, 2026

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

https://huagongshe.com/reaction/1281351

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-(4-Fluorophenoxy)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 numberUS06451830B1
Source datasetuspto-grants-2002_09
ORD IDord-4733e2d5d6564d6c85d08ed4b3d1262b
Source noteuspto-grants-2002_09