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
Participants
| Role | Name | HCID | Charge |
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| 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 | 87% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05354839 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-b9d6dd9543274ff6b6d2f3fd2edba3a1 |
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| Source note | uspto-grants-1994_10 |
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