HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methyl-4-nitrophenol → HCID 68752044, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methyl-4-nitrophenol | HCID 7442 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68752044 | HCID 68752044 | — |
Reaction Steps
To an acetonitrile (50 mL) solution of 2-methyl-4-nitrophenol (3.05 g; 19.9 mmol) and potassium carbonate (4.27 g; 30.9 mmol), 4-bromo-1-butene (4.02 g; 29.8 mmol) was added, and the mixture was refluxed and then reacted for 12 hours. After completion of the reaction, the solution was filtrated by Celite, and then 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)-2-methylnitrobenzene (1c) (2.61 g, 63% 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-9f221d2e4a7c441c862d2f3fd5e98277 |
| Source note | uspto-grants-2013_04 |