HuagongsheHuagongshe Chemistry Print Report · For research reference only
{3-[(3-Chloro-5-cyanophenyl)oxy]-2-fluoro-4-nitrophenyl}acetic acid → 3-Chloro-5-[(2-fluoro-3-methyl-6-nitrophenyl)oxy]benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | {3-[(3-Chloro-5-cyanophenyl)oxy]-2-fluoro-4-nitrophenyl}acetic acid | HCID 59451579 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Chloro-5-[(2-fluoro-3-methyl-6-nitrophenyl)oxy]benzonitrile | HCID 59451548 | 87% |
Reaction Steps
The crude {3-[(3-chloro-5-cyanophenyl)oxy]-2-fluoro-4-nitrophenyl}acetic acid was dissolved in CH3CN (50 mL) and Cu2O (0.65 g, 4.5 mmol) was added. A condenser was attached and the heterogeneous mixture was heated to reflux for 2 h. The reaction mixture was cooled to RT, filtered through Celite and the solvent evaporated. Purification was accomplished by column chromatography (hexane/EtOAc) to afford the title compound (6.0 g, 87%), which solidified upon standing. 1H NMR (400 MHz, DMSO-d6): δ ppm 7.98 (dd, 1H), 7.81 (d, 1H), 7.60 (d, 2H), 7.52 (t, 1H), 2.37 (d, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08304419B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-2641825a6ea347cc826752d5abda73d1 |
| Source note | uspto-grants-2012_11 |