HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → N-(4-cyano-2-fluoro-5-(trifluoromethyl)phenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-[4-Bromo-2-fluoro-5-(trifluoromethyl)phenyl]acetamide | HCID 23274446 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(4-cyano-2-fluoro-5-(trifluoromethyl)phenyl)acetamide | HCID 68292028 | 56.9% |
Reaction Conditions
| Temperature | 150 °C |
|---|
Reaction Steps
A mixture of compound 23 (300 mg, 1 mmol), CuCN (355 mg, 4 mmol) in DMF (6 mL) was heated at 150° C. under N2 overnight. The reaction mixture was cooled to room temperature and then poured into ice water. EtOAc was added and the insoluble solid was filtered off (rinsed with EtOAc). The organic layer was separated, and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with aq.NaHCO3 and brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified with silica gel chromatography (PE:EtOAc=4:1) to afford the title compound 24 (140 mg, 28%) as a white solid. 1H NMR (400 MHz, CDCl3) δ8.99 (d, 1H, J=7.2 Hz), 7.55 (d, 1H, J=10.0 Hz), 2.92 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09216957B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-fde8eaaa87d243409581d7a5eada02e4 |
| Source note | uspto-grants-2015_12 |