HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(5-bromo-2,4-difluorophenyl)-2-methylpropanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Reactant | 5-Bromo-2,4-difluoroaniline | HCID 2783295 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(5-bromo-2,4-difluorophenyl)-2-methylpropanamide | HCID 16757161 | 94% |
Reaction Steps
Into a solution of 2.6 g (12.6 mmol) of 5-bromo-2,4-difluoroaniline and 2.1 mL (15.1 mmol) of triethylamine in 50 mL THF at 0° C. was slowly added 1.6 mL (15.1 mmol) of isobutyryl chloride. The reaction mixture was stirred at room temperature for 2 hours and concentrated in vacuo. The residue was dissolved in EtOAc and washed with H2O, saturated aqueous Na2CO3 and brine. The organic layer was dried over MgSO4 and concentrated in vacuo to give 3.3 g (11.8 mmol, 94%) of N-(5-bromo-2,4-difluorophenyl)-2-methylpropanamide: ESMS m/e: 278.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07199135B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-cd842e07ce064aa2af7191fd639a8802 |
| Source note | uspto-grants-2007_04 |