HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Methoxy-3-nitrophenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 2-(4-Methoxy-3-nitrophenyl)acetate | HCID 7048455 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Methoxy-3-nitrophenol | HCID 14958907 | — |
Reaction Steps
4-Methoxy-3-nitrophenylacetate (2.46 g, 11.7 mmol) was dissolved in anhydrous ethanol (80 ml) and sodium ethoxide (1.19 g, 17.5 mmol) was added. The reaction was stirred at room temperature for 0.5 h. The dark red solution was acidified with 2M HCl and concentrated under reduced pressure. The residue was taken up into water and extracted with dichloromethane. The combined organics were washed with 2M HCl and brine, then dried over sodium sulfate. Evaporation of the solvent under reduced pressure gave the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07776869B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-8f04ea8b92bf4179a9e4cff06f4513de |
| Source note | uspto-grants-2010_08 |