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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Bis(3-nitrophenoxy)-5-trifluoromethylbenzene | HCID 18692419 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | 1,3-Bis(3-aminophenoxy)-5-trifluoromethylbenzene | HCID 18354084 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06103860 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-267bd2d811d64ec5ae9a5dddeaeec1a4 |
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| Source note | uspto-grants-2000_08 |
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