HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-Amino-4'-octylbiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 67059819 | HCID 67059819 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Amino-4'-octylbiphenyl | HCID 5244420 | 67% |
Reaction Steps
4′-Nitro-4-n-octyl-biphenyl (1.2 g, 3.9 mmol) was added to a suspension of palladium on carbon (Pd/C, 1.0 g) in a mixed solvent of THF (60 mL) and ethanol (24 mL). The preparation was hydrogenized under constant hydrogen flow for 3 hours. The catalyst was filtered out, and the volatiles were removed in vacuo to give a pale yellow oil. Chromatography on silica gel gave 4-n-octyl-4′-amino-biphenyl as a colorless oil, which solidified upon standing (0.75 g, 67% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902363B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-392a9e8d1abd429bb125bcd09ead2e94 |
| Source note | uspto-grants-2011_03 |