HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrophenol → Methyl 2-(2-(4-nitrophenoxy)ethoxy)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl (2-bromoethoxy)acetate | HCID 18946503 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 2-(2-(4-nitrophenoxy)ethoxy)acetate | HCID 59253929 | 43.6% |
Reaction Steps
To a mixture of 4-nitrophenol (5 g, 36 mmol), anhydrous K2CO3 (20 g, 145 mmol) and sodium iodide (2 grams, 13.3 mmol) in anhydrous acetone (100 ml) was added (2-bromoethoxy) acetic acid methyl ester (11 g, 56 mmol) and refluxed for 24 hours. Acetone was distilled off and water (100 ml) was added. Crude 22 was filtered, dried and purified by column chromatography on silica gel using benzene as eluant to give pure 22 (4 g, 43.6%) as a white fluffy powder. The melting point was found to be 96-97.8° C. The structure was confirmed with IR and NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE045548E1 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-f10e27a7d1814e699032e9263602a263 |
| Source note | uspto-grants-2015_06 |