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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871576Generated: November 1, 2026

1,3-Bis(3-nitrophenoxy)-5-trifluoromethylbenzene → 1,3-Bis(3-aminophenoxy)-5-trifluoromethylbenzene

https://huagongshe.com/reaction/1871576

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Bis(3-nitrophenoxy)-5-trifluoromethylbenzeneHCID 18692419—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Solvent2-MethoxyethanolHCID 8019—
Product1,3-Bis(3-aminophenoxy)-5-trifluoromethylbenzeneHCID 18354084—

Reaction Conditions

Temperature90 °C

Reaction Steps

Into a reducing device equipped with a thermometer, a reflux condenser and an agitator were charged 55 g of 1,3-bis(3-nitrophenoxy)-5-trifluoromethylbenzene (0.131 mol), 150 g of methyl cellosolve and 5 g of 5%-Pd/C (50% of water content), and the mixture was reacted at 70 to 80° C. for 4 hours in an atmosphere of hydrogen. At the end of the reaction, the catalyst was filtered out and the filtrate was heated to 90° C., to which 140 g of water was added. The mixture was cooled to room temperature to crystallize the desired product, which was filtered and dried under a reduced pressure to give 1,3-bis(3-aminophenoxy)-5-trifluoromethylbenzene as a white solid; Melting point: 98.0 to 98.6° C., Yield: 41 g (87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06103860
Source datasetuspto-grants-2000_08
ORD IDord-267bd2d811d64ec5ae9a5dddeaeec1a4
Source noteuspto-grants-2000_08