HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrophenol → 4-(3-Butenyloxy)nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(3-Butenyloxy)nitrobenzene | HCID 11217769 | — |
Reaction Steps
To an acetonitrile (20 mL) solution of 4-nitrophenol (0.423 g; 3.04 mmol) and potassium carbonate (1.11 g; 8.02 mmol), 4-bromo-1-butene (0.827 g; 6.13 mmol) was added, and the mixture was refluxed and then reacted for 17 hours. After completion of the reaction, the solution was filtrated by Celite, and then the filtrate was concentrated under a reduced pressure. The residue was purified by flash column chromatography using methylene chloride, and then the effluent was concentrated to obtain 4-(3-butenyloxy)nitrobenzene (1) (0.571 g, 97% of yield, a light yellow oil) represented by the following formula.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08415451B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-8e893467d62f41b6a57c287f23c04925 |
| Source note | uspto-grants-2013_04 |