HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Methyl 3-bromo-2-fluorobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | 3-Bromo-2-fluorobenzoic acid | HCID 2736313 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-bromo-2-fluorobenzoate | HCID 21584505 | 89.5% |
Reaction Steps
To a 100 mL round bottom flask was added 3-bromo-2-fluorobenzoic acid (5.00 g, 22.8 mmol, Oakwood), potassium carbonate (3.17 g, 22.9 mmol), and DMF (30 mL). Iodomethane, 2 M in MTBE (11.6 ml, 23.2 mmol) was added and the reaction mixture was stirred at RT for 16 hours. The reaction was filtered and the filtrate concentrated was in vacuo. The resulting brown crude residue was taken up with EtOAc and again filtered and concentrated to give methyl 3-bromo-2-fluorobenzoate (4.76 g, 20.4 mmol, 89.5% yield), as a brown syrup that was used in the Step 2 without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07838676B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-6f3bda2a993f464c88614095c260e517 |
| Source note | uspto-grants-2010_11 |