HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoroaniline → 5-Bromo-3,4-difluoro-2-((2-fluorophenyl)amino)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoroaniline | HCID 9584 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 5-Bromo-2,3,4-trifluorobenzoic acid | HCID 11118637 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Bromo-3,4-difluoro-2-((2-fluorophenyl)amino)benzoic acid | HCID 59519388 | 72% |
Reaction Steps
To a solution of 2-fluoro-aniline (177 mmol, 17.0 ml) in THF (80 mL) at −78° C. was added LiHMDS (265 mmol, 265 ml) and stirred for 30 min. To the reaction was added a solution of 5-bromo-2,3,4-trifluorobenzoic acid (78.4 mmol, 20.1 g) in THF (60 ml) at −78° C. The reaction was warmed to room temperature and stirred at the temperature over night. The reaction is concentrated and slowly 10% HCl (180 ml) is added. The mixture was extracted with ethyl acetate (100 ml×3), dried over MgSO4 and concentrated under reduced pressure. The crude material was taken in CH2CH2 (˜250 ml) and heated up to 45° C. for 10 min. Purification by trituration with CH2Cl2 gave 11 g (72%) of the desired product as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063049B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-cf9e890480a4466ea63d5e92edc7b591 |
| Source note | uspto-grants-2011_11 |