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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238318Generated: October 25, 2026

4-Fluoro-2-nitro-1-propoxybenzene → 5-Fluoro-2-propoxyaniline

https://huagongshe.com/reaction/238318

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluoro-2-nitro-1-propoxybenzeneHCID 66917174—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Product5-Fluoro-2-propoxyanilineHCID 2618963386%

Reaction Steps

4-Fluoro-2-nitro-1-propoxybenzene (2.0 g, 10.0 mmol) and 5% palladium carbon (750 mg) were added to ethanol (30 ml). Catalytic reduction was conducted at room temperature and atmospheric pressure (normal pressure). The catalyst was removed by celite filtration, and the filtrate was concentrated under reduced pressure. The residue was dissolved in dichloromethane, and dried over anhydrous magnesium sulfate. The resulting dry product was concentrated under reduced pressure to thereby obtain 1.45 g of oily red orange 5-fluoro-2-propoxyaniline (yield: 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642619B2
Source datasetuspto-grants-2014_02
ORD IDord-2bca2d29664e45108427f2b2d3dd0d37
Source noteuspto-grants-2014_02