HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → Ethyl 4-(2-nitrophenoxy)butanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | 2-Nitrophenol | HCID 6947 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Reactant | 2-Benzyloxyphenol | HCID 80459 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 4-(2-nitrophenoxy)butanoate | HCID 12433959 | 96% |
Reaction Steps
To a stirred solution of 2-nitrophenol. (1) (1.4 g, 10 mM) and ethyl 4-bromobutyrate (2.1 g, 1.57 mL, 11 mM) in 35 mL of dry acetone is added 2 g (14.5 mM) of anhydrous, ground potassium carbonate. The resultant colored mixture is then heated under a nitrogen atmosphere at gentle reflux until the color due to the phenol anion has dissipated and a yellow mixture remains. Concentration of the cooled and filtered mixture yields an oil which on flash chromatography (silica gel, ethyl acetate/hexane- or methylene chloride as eluant) yields 2.4 g (96% yield) of the title compound (3) as an oily liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05994362 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-e1e57e9ae72642b49c26a7ca69e215d2 |
| Source note | uspto-grants-1999_11 |