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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707730Generated: October 30, 2026

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

https://huagongshe.com/reaction/1707730

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 1835408487%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a reducing apparatus equipped with a thermometer, reflux condenser and stirrer, 55 g (0.131 mol) of 1,3-bis(3-nitrophenoxy)-5-trifluoromethylbenzene, 150 g of methyl cellosolve and 5 g of 5% Pd/c having a moisture content of 50% were charged and reacted in a hydrogen atmosphere at 70°~80° C. for 4 hours. After finishing the reaction, the catalyst was filtered off. The filtrate was heated to 90° C., mixed with 140 g of water and cooled to room temperature. The precipitated crystals were filtered and dried under reduced pressure to obtain 1,3-bis(3-aminophenoxy)-5-trifluoromethyl benzene as colorless solid. The product was 41 g (87% yield) and had a melting point of 98.0°~98.6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05354839
Source datasetuspto-grants-1994_10
ORD IDord-b9d6dd9543274ff6b6d2f3fd2edba3a1
Source noteuspto-grants-1994_10