Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Naphthol | HCID 8663 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,6-Difluorobenzonitrile | HCID 74695 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 55374169 | HCID 55374169 | 106.9% |
Reaction Steps
To a 20 mL vial containing a magnetic stir bar was added sodium hydride (103.7 mg, 4.32 mmol, 60% in mineral oil) followed by anhydrous DMF (2 mL) resulting in gas evolution. To this stirring reaction mixture was added 2-naphthol (623 mg, 4.32 mmol) as a solid in small portions over 5 min. The mixture was stirred at room temperature for 3 min and then 2,6-difluorobenzonitrile (601 mg, 4.32 mmol) in anhydrous DMF (4 mL) was added in one portion. The reaction mixture was heated in an oil bath at 100 ° C. for a total of 2 h and allowed to cool to room temperature. The reaction mixture was diluted with water (15 mL) and the resulting mixture was extracted with EtOAc (2×20 mL). The combined organic extracts were washed with water (3×20 mL), dried (Na2SO4), filtered and concentrated to give K-1 as brown solid (1.216 g) of sufficient purity (contained 2-naphthol) to be used in the subsequent step. 1H NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07714017B2 |
|---|
| Source dataset | uspto-grants-2010_05 |
|---|
| ORD ID | ord-b79c3e4f0d234aa480cf2c20b0cc463c |
|---|
| Source note | uspto-grants-2010_05 |
|---|