HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 5-Ethyl-2-[(6-fluoropyridin-2-yl)oxy]phenyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Ethyl-2-[(6-fluoropyridin-2-yl)oxy]phenol | HCID 16752719 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Ethyl-2-[(6-fluoropyridin-2-yl)oxy]phenyl acetate | HCID 59191325 | 34% |
Reaction Steps
To a solution of 5-Ethyl-2-(6-fluoro-pyridin-2-yloxy)-phenol (20 mg; 0.09 mmol), under argon, in dimethylformamide (2 mL), cooled to 0° C., was added triethylamine (36 μL; 0.26 mmol) and acetic acid (10 μL; 0.18 mmol). The reaction mixture was allowed to stir overnight, with gradual warming to room temperature. The reaction was concentrated, diluted with saturated NaHCO3 (5 mL) and extracted with ethyl acetate (3*3 mL). Combined organic phases were dried over Na2SO4, concentrated in vacuo, the title compound (8 mg; 34%) was obtained as clear oil, after purification on neutral alumina gel (cyclohexane/ethyl acetate: 9/1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09309179B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-f0677d5cfce4456da5f902b4248c4015 |
| Source note | uspto-grants-2016_04 |