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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167456Generated: October 26, 2026

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

https://huagongshe.com/reaction/2167456

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 numberUS09045464B2
Source datasetuspto-grants-2015_06
ORD IDord-d7faf677e2ee4ac080ffcec65e377450
Source noteuspto-grants-2015_06