HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methoxyphenol → p-(p-Nitrophenoxy)anisole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methoxyphenol | HCID 9015 | — |
| Reactant | 1-Bromo-4-nitrobenzene | HCID 11466 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Catalyst | Copper | HCID 23978 | — |
| Product | p-(p-Nitrophenoxy)anisole | HCID 80637 | 30.9% |
Reaction Steps
4-Bromonitrobenzene (4.0 g), hydroquinone monomethyl ether (3.1 g), potassium hydroxide (1.5 g) and copper powder (0.1 g) were mixed and the reaction was carried out at 160° C. to 200° C. for 3 hours. After cooling to room temperature, the reaction mixture was extracted with benzene (100 ml), and the extract was washed with 1 N sodium hydroxide, water, and saturated aqueous sodium chloride After drying over magnesium sulfate, the solvent was evaporated under a reduced pressure and the residue obtained was purified by medium pressure column chromatography using silica gel, to obtain 4-(4-nitrophenoxy)phenol methyl ether (1.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05205855 |
| Source dataset | uspto-grants-1993_04 |
| ORD ID | ord-3d4be8bb13cb48f28d3fca89e414599a |
| Source note | uspto-grants-1993_04 |