HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 6-Ethyl-2-(3-formyl-2-methoxy-phenoxy)-nicotinonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 3-Hydroxy-2-methoxybenzaldehyde | HCID 11804953 | — |
| Reactant | 2-Chloro-6-ethylnicotinonitrile | HCID 21930433 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Ethyl-2-(3-formyl-2-methoxy-phenoxy)-nicotinonitrile | HCID 21930392 | 62% |
Reaction Steps
2-Chloro-6-ethylnicotinonitrile (0.27 g, 1.6 mmol), 3-hydroxy-2-methoxybenzaldehyde (0.25 g, 1.6 mmol) and potassium fluoride (0.29 g, 4.9 mmol) were heated with stirring in dry DMF (4 mL) at 120° C. for 6 h, then at 80° C. for 16 h. The reaction mixture was cooled, poured into 1N sodium hydroxide solution and extracted with ethyl acetate. The ethyl acetate layer was separated, washed with 1N sodium hydroxide solution (3×), water (4×); brine (1×), and dried over MgSO4. After filtration, the solvent was removed in vacuo to yield 6-ethyl-2-(3-formyl-2-methoxy-phenoxy)-nicotinonitrile (0.28 g, 61%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07119122B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-fdc429e3e4f94c738cbfdc77ff96c303 |
| Source note | uspto-grants-2006_10 |