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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570682Generated: October 26, 2026

1-Nitro-4-(2,2,2-trifluoroethoxy)benzene → 4-(2,2,2-Trifluoroethoxy)aniline

https://huagongshe.com/reaction/570682

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Nitro-4-(2,2,2-trifluoroethoxy)benzeneHCID 2775769—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product4-(2,2,2-Trifluoroethoxy)anilineHCID 277711994.7%

Reaction Steps

1-Nitro-4-(2,2,2-trifluoroethoxy)benzene (5.5 g) was dissolved in methanol (100 ml), 10% palladium/activated carbon (50% in water, 2.5 g) was added thereto, and the mixture was stirred at room temperature for 24 hr under a hydrogen atmosphere. The palladium/activated carbon was removed by filtration, and the filtrate was concentrated under reduced pressure to give a dark orange oil residue. The obtained residue was dissolved in ethyl acetate (200 ml), and the solution was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained dark orange oil residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (4.5 g) as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023858B2
Source datasetuspto-grants-2015_05
ORD IDord-2a6120c365e848ea9e2a60e59fb32e8b
Source noteuspto-grants-2015_05