HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-(1-Trifluoromethylheptyloxy)nitrobenzene → p-(1-Trifluoromethylheptyloxy)-aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-(1-Trifluoromethylheptyloxy)nitrobenzene | HCID 15123947 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | p-(1-Trifluoromethylheptyloxy)-aniline | HCID 15123948 | — |
Reaction Steps
To 100 ml of dry ethanol containing 77.7 g of oa p-(1-trifluoromethyl-heptyloxy)-nitrobenzene, was added 0.5 g of 5% Pd/C (5% palladium carbon) followed by carrying out reduction within an atmosphere of hydrogen at normal pressure under stirring at room temperature. After it was confirmed that no absorption of hydrogen was observed, the catalyst was removed by filtration and then the ethanol was distilled off to obtain 6.7 g of oily oa p-(1-trifluoromethylheptyloxy)-aniline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05290478 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-bd92b8dd6add4baaa6f77ebbbb3a8fef |
| Source note | uspto-grants-1994_03 |