HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-(3-Bromo-4-formyl-phenoxy)-4-trifluoromethyl-benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Fluoro-4-(trifluoromethyl)benzonitrile | HCID 518973 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 2-Bromo-4-hydroxybenzaldehyde | HCID 11084866 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(3-Bromo-4-formyl-phenoxy)-4-trifluoromethyl-benzonitrile | HCID 21930341 | 96% |
Reaction Steps
2-Fluoro-4-trifluoromethyl-benzonitrile (3.1 g, 20 mmol), 2-bromo-4-hydroxybenzaldehyde (4 g, 20 mmol) and potassium fluoride-(3.47 g, 60 mmol) were heated with stirring in dry DMF (20 mL) at 120° C. for 4 h, 80° C. for 16 h, 120° C. for 4 h, 130° C. for 1 h, and then at 140° C. for 16 h. The reaction mixture was cooled, poured onto 1N sodium hydroxide, extracted with ethyl acetate, and then dried over MgSO4. After filtration, the solvent was removed in vacuo to yield 2-(3-bromo-4-formyl-phenoxy)-4-trifluoromethyl-benzonitrile (6.38 g, 96%) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07119122B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-be2dd77a220c4b6195246bc332f520ef |
| Source note | uspto-grants-2006_10 |